Variants linked to Height

Continuously updated · newest added Oct 24, 2026

10,072 positions on this site are linked to Height, out of 115,842 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)

CROCCP3 · rs115126324

See detailed info →
Standard

Height

PENK · rs112083368

See detailed info →
Standard

Height

near LINC02409 · rs11108863

See detailed info →
Standard

Height

near CRB2 · rs10985976

See detailed info →
Standard

Height

TRPM3 · rs10746850

See detailed info →
Standard

Height (baseline)

SFRP4 · rs1052974

See detailed info →
Standard

Height

near GALNT15 · rs9861567

See detailed info →
Standard

Height

TRAK1 · rs9847688

See detailed info →
Standard

Height

REM2 · rs8014119

See detailed info →
Standard

Height (baseline)

near RPS20P10 · rs78479673

See detailed info →
Standard

Height (standard GWA)

LCORL · rs77998009

See detailed info →
Standard

Height (baseline)

CROCC · rs7798

See detailed info →
Standard

Height (baseline)

SLC6A13 · rs77747027

See detailed info →
Standard

Height (baseline)

UBE3D · rs77449736

See detailed info →
Standard

Height (baseline)

IFT140 · rs76393829

See detailed info →
Standard

Height (baseline)

AAK1 · rs76371146

See detailed info →
Standard

Height (standard GWA)

CCDC26 · rs76029466

See detailed info →
Standard

Height (baseline)

IGF2BP1 · rs72833639

See detailed info →
Standard

Height (baseline)

near C17orf67 · rs7219027

See detailed info →
Standard

Height

near RBM24 · rs6910248

See detailed info →

Showing 20 of 10072 · page 92 of 504

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.