Specialist Genomic Advisory · Greater Kailash, New Delhi

Know Your DNA.
Before It Matters.

Alanine Genomics Clinic

"Your DNA. Your Story."

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Our Services

Two Focused, Life-Changing Services

We offer evidence-based genomic counselling and targeted genetic testing — keeping our practice focused so every patient receives expert, unhurried attention.

Service 01 — Cancer Genetics

Cancer Risk Gene Testing

BRCA · Lynch Syndrome · Hereditary Cancers

1 in 400
Indians estimated to carry a BRCA mutation
5–10%
of all breast & ovarian cancers are hereditary
70%
of hereditary cancers are preventable with early knowledge
#1
Breast cancer is now India's most common cancer in women

The Indian Context

Hereditary breast and ovarian cancer driven by BRCA1/BRCA2 mutations is significantly underdiagnosed in India. Certain communities — Punjabi, Bengali, Sindhi, and South Indian — carry founder mutations that are not captured in Western databases.

Lynch Syndrome, which predisposes to colorectal, endometrial, and ovarian cancers, is responsible for up to 3–5% of all colorectal cancers. Most families carrying Lynch mutations in India remain unaware.

Who Should Be Tested?

  • Breast cancer diagnosed under age 50
  • Two or more close relatives with breast or ovarian cancer
  • Ovarian cancer at any age in a blood relative
  • Male breast cancer in the family
  • Triple-negative breast cancer (any age)
  • Two or more primary cancers in same individual
  • Colorectal cancer with family clustering
  • Punjabi, Bengali, or South Indian ancestry

What We Screen For

Gene / Panel Cancer Risk Covered Recommended For
BRCA1 / BRCA2 Breast, Ovarian, Pancreatic, Prostate First-line for all women with family history
MLH1, MSH2, MSH6, PMS2 (Lynch Panel) Colorectal, Endometrial, Ovarian, Gastric Colorectal family clustering; early-onset CRC
PALB2, CHEK2, ATM Breast, Pancreatic (moderate–high risk) BRCA-negative with strong family history
Hereditary Cancer Panel (25+ genes) Comprehensive multi-cancer risk assessment Complex family history; multiple cancer types
Cascade Testing (known variant) Single variant confirmation in relatives Family members of a known positive carrier

After Your Test — What Happens Next

01
Pre-Test Counselling
Review of personal and family history. Selecting the right gene panel for your risk profile.
02
Blood Draw & Lab Processing
Simple 5 ml blood sample. Processed by NABL-accredited partner labs. Results in 14–21 days.
03
Results & Action Plan
Personal result session with your genomic counsellor. Surveillance plan, specialist referrals, and cascade testing for family.

Approximate Costs (INR)

Test Approx. Cost Notes
BRCA1 / BRCA2 (2-gene panel) ₹ 8,000 – 12,000 Most common first-line test
Lynch Syndrome Panel (4 genes) ₹ 12,000 – 18,000 For colorectal/endometrial family history
Hereditary Cancer Panel (25+ genes) ₹ 22,000 – 35,000 Broad multi-cancer coverage
Cascade Testing (family member) ₹ 3,500 – 6,000 Single known variant; discounted rate
Genetic Counselling (per session) ₹ 500 – 1,500 Pre- and post-test consultation
Service 02 — Pre-Marital Genetics

Pre-Marital Genetic Counselling

Thalassaemia · Sickle Cell · Carrier Screening

India registers 10,000–12,000 new Thalassaemia Major births every year. An estimated 42 million Indians carry the Thalassaemia gene — most without knowing. Every one of these births is preventable with a simple blood test before marriage.
4.2 Cr
Indians carry the Thalassaemia gene
25%
risk per pregnancy when both partners are carriers
1.5 Cr
estimated Sickle Cell carriers across India
100%
of these births are preventable with pre-marital screening

Why Screen Before Marriage?

Haemoglobin disorders are autosomal recessive — carriers are completely healthy and have no symptoms. Two carriers can only be identified through a blood test. When two carriers marry, every pregnancy carries a 1-in-4 chance of producing a severely affected child.

Pre-marital genetic screening identifies this risk before conception, giving couples full information and reproductive choices — including prenatal diagnosis, PGT-M, or adoption.

Who Should Consider This?

  • All couples planning marriage — ideally 3–6 months before
  • Families with any relative with Thalassaemia or Sickle Cell
  • Punjabi, Sindhi, Bengali, Gujarati ancestry (higher Thal rates)
  • Banjara, tribal, or Scheduled Tribe communities (Sickle Cell)
  • Anyone told they have "mild anaemia not responding to iron"
  • Couples with a previous child with unexplained anaemia

What We Screen For

Condition Test Used Risk (Both Carriers)
Beta Thalassaemia HPLC + Genetic mutation panel 25% per pregnancy (Thal Major)
Sickle Cell Anaemia HPLC + HbS mutation confirmation 25% per pregnancy (SCD)
G6PD Deficiency Enzyme assay + molecular testing 50% of sons affected (X-linked)
Spinal Muscular Atrophy (SMA) SMN1 copy number analysis 25% per pregnancy (severe)
Cystic Fibrosis CFTR mutation panel 25% per pregnancy

Our Counselling Process

01
Joint Consultation
Both partners attend together. Family history review, risk assessment, and test selection.
02
Blood Sampling
Simple 5 ml blood draw for each partner. No fasting required. NABL lab processing. Results in 7–14 days.
03
Results & Options
Personal result session. If carrier couple: full discussion of reproductive options, prenatal diagnosis, and next steps.

Approximate Costs (INR)

Test Approx. Cost Notes
HPLC (Haemoglobinopathy screen, per person) ₹ 800 – 1,500 Primary carrier screen — start here
Couple Package (HPLC x2 + Counselling) ₹ 3,000 – 4,500 Best-value entry for both partners
Beta Thalassaemia Mutation Panel ₹ 3,500 – 6,000 Identifies exact mutation for prenatal diagnosis
Sickle Cell (HbS) Confirmation ₹ 2,000 – 3,500 Molecular confirmation of HbS variant
G6PD Enzyme Assay ₹ 600 – 1,200 Especially relevant for male partners
SMN1 Copy Number (SMA Carrier) ₹ 4,500 – 7,000 Recommended for North Indian communities
CFTR Panel (Cystic Fibrosis) ₹ 5,000 – 8,000 Punjabi / NW Indian ancestry
SKB
Dr. Satish K. Bhardwaj
MD · FACEE
AHA ACLS/BLS Instructor
PhD Scholar — Oncogenomics
30+ Years Clinical Experience
About Your Doctor

Three Decades of Medicine.
Now at the Frontier of Genomics.

Dr. Satish K. Bhardwaj brings over 30 years of clinical experience as a senior Emergency Medicine specialist to the emerging field of genomic medicine. Currently serving as Incharge of Emergency Medicine & Clinical Training at Kailash Hospital Group across Delhi NCR, he has witnessed firsthand the devastating — and often preventable — impact of undetected hereditary disease.

Driven by this, Dr. Bhardwaj is currently pursuing a PhD in Cellular and Molecular Oncology (Oncogenomics) at Amity University, Noida, with active research in ctDNA-based liquid biopsy and CBC-derived inflammatory biomarkers in oncological emergencies. Alanine Clinic is the clinical expression of this research — bringing cutting-edge genomic science directly to patients.

His practice philosophy is simple: a single informed test today can protect not just you, but your children and grandchildren.

  • MD — Emergency Medicine
  • FACEE (Fellow, Emergency Medicine)
  • AHA ACLS / BLS Instructor
  • PhD Scholar — Oncogenomics
  • DGCA Aviation Medical Examiner
  • 30+ Years Clinical Practice
  • Published Author — First Aid & Emergency Care
  • Kailash Hospital Group, Delhi NCR
Find Us

Visit Alanine Clinic

Clinic Address

📍
Alanine Genomics Clinic M2 Basement, Greater Kailash Part 1
New Delhi — 110 048
📞
Phone / WhatsApp +91 98114 12126
🕐
Clinic Hours By appointment · Mon – Sat

Location

📍
M2 Basement, Greater Kailash Part 1
New Delhi 110048

Near GK-1 M-Block Market
Open in Google Maps

Appointments preferred.
WhatsApp or call +91 98114 12126 to book your consultation. Same-day appointments may be available.