All variants

Continuously updated · newest added Sep 16, 2026

12,438 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.

Standard

Insulin-like growth factor 1 levels

near PRSS36 · rs112766425

See detailed info →
Standard

Urate levels

MED4 · rs2104480

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Sensitive

DPYD c.2846A>T — fluoropyrimidine tolerance

DPYD · rs67376798

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Sensitive

DPYD HapB3 — fluoropyrimidine tolerance

DPYD · rs75017182

See detailed info →
Sensitive

DPYD *2A — fluoropyrimidine tolerance

DPYD · rs3918290

See detailed info →
Sensitive

CYP2C19 *2 — clopidogrel activation

CYP2C19 · rs4244285

See detailed info →
Sensitive

CYP2C19 *3 — clopidogrel activation

CYP2C19 · rs4986893

See detailed info →
Standard

CYP2C19 *17 — increased enzyme activity

CYP2C19 · rs12248560

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Sensitive

TPMT *3C — thiopurine tolerance

TPMT · rs1142345

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Sensitive

NUDT15 *3 — thiopurine tolerance

NUDT15 · rs116855232

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Standard on its own

IgE levels

FCER1A · rs2251746

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Standard

Chronic lymphocytic leukemia

PRKD2 · rs11083846

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Standard

Triglycerides

APOC3 · rs12286037

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Standard

Ulcerative colitis

3.8-1 · rs3749946

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Sensitive

Pediatric autoimmune diseases

INS · rs17885785

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Standard

Ulcerative colitis

IL23R · rs76418789

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Standard

Ulcerative colitis

HLA · rs117506082

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Standard

Ulcerative colitis

SLC6A7 · rs17656349

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Standard

Ulcerative colitis

TOM1 · rs138788

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Standard

Ulcerative colitis

INPP5E · rs10781499

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Showing 20 of 12438 · page 602 of 622

Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.