Gene Knowledge Graph
UTC

Variants linked to Height

Continuously updated · newest added Oct 23, 2026

9,513 positions on this site are linked to Height, out of 109,292 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Clear
Newest Oldest

← Back to Height

Standard

Height

OTUD7B · rs3767627

See detailed info → Standard

Height

TOP1MT · rs2450771

See detailed info → Standard

Height (maximum, inv-normal transformed)

CDCA2 · rs11777745

See detailed info → Standard

Height (maximum, inv-normal transformed)

NAV3 · rs7137768

See detailed info → Standard

Height (baseline)

ANKRD36B · rs55788356

See detailed info → Standard

Height

CALCRL-AS1 · rs17705966

See detailed info → Standard

Height

SPAAR · rs10814297

See detailed info → Standard

Height (maximum, inv-normal transformed)

near LINC01423 · rs9976812

See detailed info → Standard

Height (baseline)

SLA2 · rs4810266

See detailed info → Standard

height (minimum, inv-normal transformed)

near SSBP3 · rs11206349

See detailed info → Standard

Height (baseline)

DIRC3 · rs74411434

See detailed info → Standard

Height

ADAMTS17 · rs1383543

See detailed info → Standard

Height (baseline)

ZRANB2 · rs66461782

See detailed info → Standard

Height (baseline)

LCORL · rs74537632

See detailed info → Standard

Standing height (UKB data field 50)

near NIP7P1 · rs117327710

See detailed info → Standard

Height

RND3 · rs2222760

See detailed info → Standard

Height

near PDE4B · rs11208844

See detailed info → Standard

Height

near TOM1L1 · rs2934901

See detailed info → Standard

Height (baseline)

PPP3R1 · rs75483778

See detailed info → Standard

Height

TTC28 · rs76450219

See detailed info →

Showing 20 of 9513 · page 442 of 476

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.