All variants

Continuously updated · newest added Sep 13, 2026

8,605 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 on its own

Hand grip strength

POU6F2 · rs4549685

See detailed info →
Standard on its own

Hand grip strength

CIR1 · rs72917544

See detailed info →
Standard on its own

Hand grip strength

HLA-DRB1 · rs2760975

See detailed info →
Standard

Glaucoma (primary open-angle)

PRKAG2 · rs62478245

See detailed info →
Standard on its own

Male-pattern baldness

STAU2 · rs11774977

See detailed info →
Standard on its own

Male-pattern baldness

near FOXF2 · rs11756214

See detailed info →
Standard on its own

Male-pattern baldness

near CDYL2 · rs117538856

See detailed info →
Standard on its own

Male-pattern baldness

near BHLHE40 · rs11715919

See detailed info →
Standard on its own

Male-pattern baldness

near KLF12 · rs11619505

See detailed info →
Sensitive

Broad depression or major depressive disorder (self-reported)

NEGR1 · rs2422320

See detailed info →
Sensitive

Broad depression or major depressive disorder (self-reported)

MUC21 · rs9368649

See detailed info →
Sensitive

Serum bilirubin levels in metabolic syndrome

UGT1A1 · rs929596

See detailed info →
Sensitive

Serum bilirubin levels in metabolic syndrome

UGT1A6 · rs2070959

See detailed info →
Sensitive

Serum bilirubin levels in metabolic syndrome

MROH2A · rs2361502

See detailed info →
Sensitive

Serum bilirubin levels in metabolic syndrome

near UGT1A8 · rs2741027

See detailed info →
Standard on its own

Body mass index

near TMEM18 · rs6725549

See detailed info →
Sensitive

Serum bilirubin levels in metabolic syndrome

UGT1A6 · rs17863787

See detailed info →
Standard on its own

Body mass index

MFAP3 · rs815610

See detailed info →
Standard on its own

Male-pattern baldness

GIN1 · rs115505614

See detailed info →
Standard on its own

Body mass index

CADM2 · rs13068138

See detailed info →

Showing 20 of 8605 · page 22 of 431

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.