Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,402 positions on this site are linked to Height, out of 108,284 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 (baseline)

LINC01645 · rs12129327

See detailed info →
Standard

Height

near ST13P19 · rs12123877

See detailed info →
Standard

Height

PBRM1 · rs12107484

See detailed info →
Standard

Height

near KLHL28 · rs117874812

See detailed info →
Standard

Height (baseline)

SPATA31H1 · rs11682583

See detailed info →
Standard

Height (baseline)

PHAF1 · rs115599330

See detailed info →
Standard

Height

near FUNDC2P2 · rs11126959

See detailed info →
Standard

Height

TMEM119 · rs11114004

See detailed info →
Standard

Height (standard GWA)

near EEF1B2P4 · rs11113137

See detailed info →
Standard

Height (baseline)

MUSK · rs10817086

See detailed info →
Standard

Height

near FUBP3 · rs10793930

See detailed info →
Standard

Height

TMTC2 · rs10778921

See detailed info →
Standard

Height

near CHCHD4P2 · rs10512362

See detailed info →
Standard

Height

ALMS1 · rs10496189

See detailed info →
Standard

Height

FAF1 · rs10218771

See detailed info →
Standard

Height

DPP10 · rs10210316

See detailed info →
Standard

Height (baseline)

RBMS3 · rs1011416

See detailed info →
Standard

Height

RASGEF1B · rs10024084

See detailed info →
Standard

Height

LINC01182 · rs10007245

See detailed info →
Standard

Height

LINC02469 · rs10002178

See detailed info →

Showing 20 of 9402 · page 25 of 471

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.