All variants

Continuously updated · newest added Sep 16, 2026

12,469 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.

Sensitive

Inflammatory bowel disease

near CTH · rs2651244

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Sensitive

Inflammatory bowel disease

near ZBTB40 · rs12568930

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Sensitive

Inflammatory bowel disease

FOS · rs4899554

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Standard

Vascular endothelial growth factor levels

KCNV2 · rs10738760

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Standard

Vascular endothelial growth factor levels

MGC45491 · rs9472155

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Standard

Vascular endothelial growth factor levels

ZFPM2 · rs6993770

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Standard

Vascular endothelial growth factor levels

MRPL14 · rs4513773

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Standard

Bilirubin levels

UGT1A1 · rs6742078

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Standard

Waist-hip ratio

RREB1 · rs6931262

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Standard

Bone mineral density (spine)

SPTBN1 · rs11898505

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Standard

LDL cholesterol

CELSR2 · rs12740374

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Sensitive

Inflammatory bowel disease

CD40 · rs1569723

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Sensitive

Inflammatory bowel disease

KIR2DL1 · rs11672983

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Sensitive

Inflammatory bowel disease

RPS6KB1 · rs1292053

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Sensitive

Inflammatory bowel disease

CEBPB · rs913678

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Standard on its own

Body mass index (SNP x SNP interaction)

FTO · rs12149832

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Standard

Body mass index

PCSK1 · rs261967

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Standard

Body mass index

CDKAL1 · rs9356744

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Sensitive

Parkinson's disease

SCARB2 · rs6812193

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Sensitive

Basal cell carcinoma

EXOC2 · rs12210050

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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.