Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,348 positions on this site are linked to Height, out of 107,684 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

HHIP · rs117072351

See detailed info →
Standard

Height (baseline)

TGFBR3 · rs115401860

See detailed info →
Standard

Height (baseline)

near KLHL22 · rs1153427

See detailed info →
Standard

Height (standard GWA)

EFCAB5 · rs114658410

See detailed info →
Standard

Height

near LINC01519 · rs11201527

See detailed info →
Standard

Height

SPSB1 · rs11121380

See detailed info →
Standard

Height

near RPSAP20 · rs10888959

See detailed info →
Standard

Height (baseline)

SYN3 · rs10854622

See detailed info →
Standard

Height (baseline)

GRB10 · rs10235705

See detailed info →
Standard

Height

ADCY1 · rs10225980

See detailed info →
Standard

Height

near SBF1P2 · rs1009592

See detailed info →
Standard

Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

LINC02227 · rs10044492

See detailed info →
Standard

Height

LINC01725 · rs9787364

See detailed info →
Standard

Height

ANO1 · rs9630219

See detailed info →
Standard

Height (baseline)

near LNX2 · rs9581878

See detailed info →
Standard

Height

BMP6 · rs9505276

See detailed info →
Standard

Height (baseline)

near HMGN1P19 · rs856586

See detailed info →
Standard

Height

ETS2-AS1 · rs8131592

See detailed info →
Standard

Height (baseline)

LINC01574 · rs812817

See detailed info →
Standard

Height

WFDC1 · rs8051764

See detailed info →

Showing 20 of 9348 · page 17 of 468

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.