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Make Informed Health Decisions with Deep DNA Insights

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Preserve
Your Good Health

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Protect From
Inheritable Diseases

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Optimised Health
Monitoring

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Peace of Mind
via Proactive Care

Why wait to get sick when diseases can be prevented years before symptoms?

What's Covered in the Test

Hereditary Cancers

Hereditary cancers result from inherited gene mutations that increase the likelihood of developing certain cancers, including breast, ovarian, colorectal, and prostate cancers. Early identification of these genetic predispositions help in taking preventive measures, such as increased screening, lifestyle adjustments, or preventive surgeries, to reduce the chance of developing cancer.

HEALTHSTRING, analyses over 800 cancer causing genes and their mutations, offering the most comprehensive preventive screening available globally.

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Blood

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Breast

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Lung

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Mouth

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Breast

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Lung

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Blood

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Thyroid

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Stomach

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Ovary

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Prostate

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Mouth

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Liver

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Bone

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Brain

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Pancreas

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Skin

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Kidney

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Heart

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Rectum

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Eye

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Colon

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Throat

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Adrenal gland

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Blood vessels

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Bone marrow

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Connective tissue

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Gastrointestinal tract

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Endocrine system

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Endometrium

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Esophagus

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Gastrointestinal tract

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Sebum gland

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Gums

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Hypothalamus

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Lymphoid tissue

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Nerves

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Pituitary gland

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Soft tissue

  • Ataxia Telangetasia
  • Ataxia Telangetasia-like Disorder
  • Bannayan-Riley-Ruvalcaba Syndrome
  • Basal Cell Nevus Syndrome
  • Birt-Hogg-Dube Syndrome
  • Bloom Syndrome
  • Breast Cancer
  • Carney Complex
  • Carney-Stratakis Syndrome
  • Chediak-Higashi Syndrome
  • Costello Syndrome
  • Cowden Syndrome
  • Denys-Drash Syndrome
  • Endometrial Cancer
  • Familial Monocytic Leukemia
  • Familial Multiple Glomus Tumors
  • Familial Multiple Trichoepithelioma
  • Familial Myeloproliferative/Lymphoproliferative Neoplasms
  • Familial Osteosarcoma
  • Familial Pancreatic Cancer
  • Familial Uveal Melanoma
  • Fanconi Anemia
  • Ferguson-Smith Syndrome
  • Gardner Syndrome
  • Glioma
  • Hemochromatosis
  • Hereditary Acute Myeloid Leukemia
  • Hereditary Adenomatous Polyposis
  • Hereditary Adrenal Hyperplasia
  • Hereditary Adrenal Pheochromocytoma
  • Hereditary Adrenocortical Cancer
  • Hereditary Barrett Esophagus/Esophageal Adenocarcinoma
  • Hereditary Bone Dysplasia with Malignant Fibrous Histiocytoma
  • Hereditary Breast-Ovarian Cancer
  • Hereditary Colorectal Cancer
  • Hereditary Desmoid Disease
  • Hereditary Epidermodysplasia Verruciformis
  • Hereditary Gastric Carcinoma
  • Hereditary GIST
  • Hereditary Hodgkin Lymphoma
  • Hereditary Infantile Hemangioma
  • Hereditary Isolated Pituitary Adenoma
  • Hereditary Leiomyomatosis & Renal Cell Cancer
  • Hereditary Lung Cancer
  • Hereditary Malignant Melanoma
  • Hereditary Medulloblastoma
  • Hereditary Melanoma & Renal Cancer
  • Hereditary Neuroblastoma
  • Hereditary Paragangliomas
  • Hereditary Pleuropulmonary Blastoma
  • Hereditary Primary Pigmented Nodular Adrenocortical Disease
  • Hereditary Prostate Cancer
  • Hereditary Thyroid Cancer
  • Hereditary Wilms’ Tumor
  • Howel-Evans syndrome
  • Hyperparathyroidism-Jaw Tumor Syndrome
  • Juvenile Hyaline Fibromatosis
  • Juvenile Polyposis Syndrome
  • Lhermitte-Duclos syndrome
  • Li-Fraumeni Syndrome
  • LIG4 Syndrome
  • Lymphangioleiomyomatosis
  • Lynch Syndrome
  • Melanoma and Neural System Tumor Syndrome
  • Melanoma-pancreatic Cancer Syndrome
  • Mismatch Repair Cancer Syndrome
  • Mosaic Variegated Aneuploidy
  • Muir-Torre Syndrome
  • Multiple Endocrine Neoplasia
  • Multiple Exostoses
  • Myelodysplastic Syndrome
  • Neurofibromatosis
  • Nijmegen Breakage Syndrome
  • Nijmegen Breakage-like Syndrome
  • Noonan Syndrome-like Disorder with or without Juvenile Myelomonocytic AD 24 43 leukemia
  • Oligodontia-Colorectal Cancer Syndrome
  • Opitz Trigonocephaly Syndrome
  • Oral Cancer
  • Pallister-Hall Syndrome
  • Palmoplantar Keratoderma & Squamous Cell Carcinoma
  • Perlman Syndrome
  • Peutz-Jeghers Syndrome
  • POLD1 & POLE Associated Colorectal Adenomas
  • Porphyria Cutanea Tarda
  • Proteus Syndrome
  • Retinoblastoma
  • Rhabdoid Predisposition Syndrome
  • Rothmund-Thompson Syndrome
  • SC Phocomelia Syndrome
  • Schwachman-Diamond Syndrome
  • Schwannomatosis
  • Seckel Syndrome 1
  • Simpson-Golabi-Behmel Syndrome
  • TERT Mutation-Associated Haematological Disorders
  • Tumor Predisposition Syndrome
  • Tyrosinemia
  • Von Hippel-Lindau Syndrome
  • Werner Syndrome
  • Wiskott-Aldrich Syndrome
  • Xeroderma Pigmentosum
Not finding what you need?
🇮🇳
+91
India
Not finding what you need?
Not finding what you need?
🇮🇳
+91
India

100% Specificity

achieved with AI/ML.

Absolute, Individualised, Actionable.

Genetic diseases are often progressive and can become life-threatening when triggered by lifestyle or environmental factors. Early risk identification enables proactive prevention.

We analyze all functional regions of the DNA using proprietary, population-agnostic, machine-learning-driven algorithms to detect variations that could lead to diseases.

With the highest sensitivity and specificity in detection, the results are presented in a clinically actionable format, adhering to international guidelines for DNA screening.

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Single-base level investigation of genetic risks.

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Population-agnostic and evidence based reporting.

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Individualised insights, enabling precise health strategies.

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Steer your life toward wellness, not illness.

Clinical-Grade Report

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Mutation (DNA Error)

Reveals the root causes and health impact.
Mutated Gene

MLH1

Disease

Lynch syndrome 2

Risk: Cancers

Raises the risk of various cancers, especially colorectal cancer.

Details of the mutation found

  • Mutation

    : 3-37020354-C-G ENST0000023 1790.8 c.929C >G p.Thr310Arg

  • Type

    : Missense

  • Zygosity

    : Heterozygous

  • Inheritance

    : Autosomal Dominant

  • Classification

    : Likely Pathogenic

Actionable insights & suggestions

Lynch syndrome is an inherited genetic condition that increases the risk of various types of cancer, particularly colorectal cancer and endometrial cancer. Lynch syndrome is caused by mutations in genes that are responsible for DNA repair...

We adhere to international guidelines, ensuring clinical actionability.

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Sample collection is effortlessly simple!
1
Rinse your mouth
Avoid eating or drinking in the last 30 minutes before taking the sample
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Collect the sample
Avoid the swab touching other surfaces to avoid contamination
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Register your kit
Dot forget to register the kit before sealing

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The preservation of health is easier than the cure of disease.

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FAQ

We sequence all the functional regions in your DNA using Next Generation DNA Sequencing technology to identify your unique genetic variants. Our proprietary AI/ML-driven algorithms analyse your DNA to detect genetic factors linked to the covered diseases.

In 4 weeks, you receive a personalised, clinical-grade genetic health report with actionable recommendations.

HEALTHSTRING™ identifies the risk of over 6,000 genetic conditions before disease onset, enabling physicians to develop preventive strategies such as lifestyle changes or medical treatments to avoid adverse health events.

Knowing potential threats in advance can optimise future health screenings, customised to your conditions, and to catch early signs well before visible signs and symptoms. Mitigate set backs in advance, and enrich your healthspan.

Such Informed decision-making at the right time maximises your potential, and staying healthy always provides more opportunities in life.

HEALTHSTRING™ uses the most advanced DNA sequencing technology, with a demonstrated accuracy of 99.9999%. Our proprietary, population-agnostic machine learning algorithms for data interpretation detect disease risks with 100% specificity.

The clinical-grade genetic health reports are prepared in accordance with international clinical guidelines prescribed by ACMG-AMP (American College of Medical Genetics and Genomics-Association for Molecular Pathology), ASCO (American Society of Clinical Oncology), and NCCN (National Comprehensive Cancer Network).

HEALTHSTRING™ delivers precise genetic health reports with 100% specificity, unlike the population-relative risk scores provided by other genetic screening products.

Our approach surpasses the outdated, marker-based methods used by others, which typically have less than 80% specificity (>20% false positives) and only 40% sensitivity (>60% false negatives). We decode every letter of targeted gene segments in your DNA, ensuring comprehensive coverage and detailed analysis.

HEALTHSTRING™’s proprietary, population-agnostic approach, powered by machine learning algorithms sets us apart. It operates independently of the genetic frequencies in public databases, which are often biased toward Caucasian populations.

HEALTHSTRING™ is suitable for anyone interested in proactively preventing life-limiting health conditions tailored to their specific needs, regardless of age, gender, or clinical history.

Those with specific health concerns, a family history of certain conditions, or individuals planning for family expansion may find these tests particularly relevant.

After placing an order, a buccal swab collection kit will be sent to your address. Follow the simple instructions in the kit to collect your sample. Once done, register the kit on the SugarStrings.ai website, and we will arrange for the sample to be picked up from your address.

HEALTHSTRING™ report will be delivered to you within 4 weeks from the date of receipt of your sample at the laboratory. Regular emails will keep you posted on the progress.

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Have more questions?
Get a callback from our team

Careers:

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+91
India
About Us

SugarStrings.ai is a deep tech multiomic platform for the prevention and management of chronic genetic conditions, including cancers. Led by genomics pioneers and product visionaries, we are committed to making genomic-based healthcare accessible to billions.

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© Precision Health Innovations pvt.ltd

India.