Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,248 positions on this site are linked to Height, out of 106,676 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 Height

Standard

Height

TLE3 · rs4777230

See detailed info →
Standard

Height

SOCS2 · rs9634212

See detailed info →
Standard

Height

CDK6 · rs42377

See detailed info →
Standard

Height

DLEU1 · rs3116614

See detailed info →
Standard

Height

LCORL · rs2061456

See detailed info →
Standard

Height

PRKG2 · rs1975474

See detailed info →
Standard

Height

RILPL2 · rs28376121

See detailed info →
Standard

Height

ACAN · rs16942323

See detailed info →
Standard

Height

near UQCC1 · rs6060402

See detailed info →
Standard

Height

ARHGAP24 · rs552283803

See detailed info →
Standard

Height

NPR3 · rs72742734

See detailed info →
Standard

Height

DAP · rs755546258

See detailed info →
Standard

Height

RP11-317P15.6 · rs558671668

See detailed info →
Standard

Height

CMTM8 · rs6765866

See detailed info →
Standard

Height

LCORL · rs35362908

See detailed info →
Standard

Height

RP1-35C21.2 · rs146949893

See detailed info →
Standard

Height

CTD-2023 N9.1 · rs554379257

See detailed info →
Standard

Height

near PPFIA2 · rs139770682

See detailed info →
Standard

Height

near PPP1R3A · rs184469050

See detailed info →
Standard

Height

KDM2A · rs7952436

See detailed info →

Showing 20 of 9248 · page 457 of 463

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.