Variants linked to Aortic Stenosis

Continuously updated · newest added Oct 10, 2026

90 positions on this site are linked to Aortic Stenosis, out of 61,233 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Aortic Stenosis

Standard

Aortic stenosis

near ISL1 · rs7713979

See detailed info →
Standard

Aortic stenosis

near CEP120 · rs7725897

See detailed info →
Standard

Aortic stenosis

near MYLK4 · rs2449447

See detailed info →
Standard

Aortic stenosis

ABL1 · rs7851994

See detailed info →
Standard

Aortic stenosis

PIP5K1B · rs1412987

See detailed info →
Standard

Aortic stenosis

near MEGF9 · rs34089221

See detailed info →
Standard

Aortic stenosis

PLEC · rs188595907

See detailed info →
Standard

Aortic stenosis

FARP1 · rs11617458

See detailed info →
Standard

Aortic stenosis

near CDK8 · rs12430162

See detailed info →
Standard

Aortic stenosis

GPC6 · rs4366594

See detailed info →
Standard

Aortic stenosis

CMKLR1 · rs141421422

See detailed info →
Standard

Aortic stenosis

FN1 · rs4328631

See detailed info →
Standard

Aortic stenosis

near CEP120 · rs11241687

See detailed info →
Standard

Aortic stenosis

PDGFRB · rs12515782

See detailed info →
Standard

Aortic stenosis

near PDE7B · rs73549085

See detailed info →
Standard

Aortic stenosis

SUFU · rs35095897

See detailed info →
Standard

Aortic stenosis

SORBS1 · rs140453415

See detailed info →
Standard

Aortic stenosis

SMAD3 · rs17228212

See detailed info →
Standard

Aortic stenosis

near MYOCD · rs35263589

See detailed info →
Standard

Aortic stenosis

WASF2 · rs111478493

See detailed info →

Showing 20 of 90 · page 4 of 5

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.