Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,908 positions on this site are linked to Height, out of 113,825 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)

near UQCC1 · rs76660268

See detailed info →
Standard

Height

FANCI · rs7168941

See detailed info →
Standard

Height (baseline)

TBX2-AS1 · rs138987744

See detailed info →
Standard

Height (baseline)

near POMC · rs34914018

See detailed info →
Standard

Height (baseline)

TSC2 · rs17654678

See detailed info →
Standard

Height

LRRC45 · rs11659000

See detailed info →
Standard

Height (baseline)

near UBE2Q2P8 · rs11636961

See detailed info →
Standard

Height

near PMP22 · rs10852830

See detailed info →
Standard

Height (baseline)

IGF2BP2 · rs189323430

See detailed info →
Standard

Height (baseline)

CLHC1 · rs138994967

See detailed info →
Standard

Height (baseline)

near ATP6V1FP1 · rs11321980

See detailed info →
Standard

Height (baseline)

near RNU6-221P · rs76416108

See detailed info →
Standard

Height (baseline)

CNBD2 · rs76382038

See detailed info →
Standard

Height (baseline)

CC2D1B · rs41294498

See detailed info →
Standard

Height (baseline)

near MTCH2 · rs147238791

See detailed info →
Standard

Height (baseline)

STRADA · rs139188744

See detailed info →
Standard

Standing height (UKB data field 50)

TGFB3 · rs11466414

See detailed info →
Standard

Standing height (UKB data field 50)

SUPT3H · rs145364349

See detailed info →
Standard

Height (baseline)

near HECTD2-AS1 · rs11595984

See detailed info →
Standard

Height

CNIH4 · rs11586729

See detailed info →

Showing 20 of 9908 · page 421 of 496

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.