Variants linked to Height

Continuously updated · newest added Oct 23, 2026

9,593 positions on this site are linked to Height, out of 110,301 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

CCDC66 · rs17825523

See detailed info →
Standard

Height

near LINC01713 · rs6038579

See detailed info →
Standard

Height

LINC00243 · rs1264353

See detailed info →
Standard

Height

near LZTS2 · rs10883567

See detailed info →
Standard

Height

near FOXD2 · rs543640

See detailed info →
Standard

Height

XRCC1 · rs25484

See detailed info →
Standard

Height

DLEU1 · rs706615

See detailed info →
Standard

Height

near RNA5SP94 · rs13005495

See detailed info →
Standard

Height

near CASC9 · rs16939031

See detailed info →
Standard

Height

RALGAPA1 · rs1169031

See detailed info →
Standard

Height

TGFB2 · rs6662137

See detailed info →
Standard

Height

ATF7IP · rs10845987

See detailed info →
Standard

Height

near LINC00620 · rs6786420

See detailed info →
Standard

Height

DDX6 · rs581045

See detailed info →
Standard

Height

CAMKMT · rs17390720

See detailed info →
Standard

Height

near RN7SKP15 · rs7304170

See detailed info →
Standard

Height

MICA-AS1 · rs7775759

See detailed info →
Standard

Height

ATXN10 · rs136029

See detailed info →
Standard

Height

TRA2B · rs2300921

See detailed info →
Standard

Height

near SDC1 · rs6749689

See detailed info →

Showing 20 of 9593 · page 437 of 480

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.