All variants

Continuously updated · newest added Sep 12, 2026

7,519 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

Ulcerative colitis

INPP5E · rs10781499

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Standard

Ulcerative colitis

TNPO3 · rs4728142

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Standard

Ulcerative colitis

IL7R · rs3194051

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Standard

Ulcerative colitis

IL10 · rs3024505

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Standard

Ulcerative colitis

HLA-DRA · rs9268923

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Standard

Ulcerative colitis

NOTCH4 · rs549182

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Standard

Ulcerative colitis

C1orf106 · rs7554511

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Standard

Ulcerative colitis

IFNG · rs1558744

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Standard

Ulcerative colitis

HLA · rs9263739

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Sensitive

Pediatric autoimmune diseases

LRRK2 · rs17466626

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Sensitive

Pediatric autoimmune diseases

SUOX · rs1689510

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Sensitive

Pediatric autoimmune diseases

NOD2 · rs117372389

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Sensitive

Pediatric autoimmune diseases

FUT2 · rs602662

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Sensitive

Pediatric autoimmune diseases

PSMG1 · rs2836882

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Standard

Ulcerative colitis

C6orf10 · rs2395185

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Standard

Ulcerative colitis

PSMG1 · rs2836878

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Standard

Ulcerative colitis

NKX2-3 · rs11190140

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Standard

Ulcerative colitis

PUS10 · rs13003464

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Sensitive

Ulcerative colitis or Crohn's disease

TNFSF15 · rs2006996

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Standard

Ulcerative colitis

CALM3 · rs1126510

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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.