Gene Knowledge Graph
UTC

Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 8, 2026

10,926 positions on this site are linked to Height, out of 2,505,478 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Clear
Recommended (connected, strongest) Strongest evidence Newest Oldest

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

PTPN4 · rs3111728

See detailed info → Standard

Height

ACO2 · rs2076196

See detailed info → Standard

Height

RUNX3-AS1 · rs11249209

See detailed info → Standard

Height

near ANXA1 · rs9314803

See detailed info → Standard

Height

near LEF1-AS1 · rs852269

See detailed info → Standard

Height

SLC45A4 · rs6578155

See detailed info → Standard

Height

CPM · rs3741598

See detailed info → Standard

Standing height (UKB data field 50)

MIR4713HG · rs16964220

See detailed info → Standard

Height

ADGRL1 · rs12971709

See detailed info → Standard

Height

FAF1 · rs12089747

See detailed info → Standard

Height

ROCR · rs7217914

See detailed info → Standard

Height

AP1M2 · rs2304160

See detailed info → Standard

Height

CBFA2T2 · rs209665

See detailed info → Standard

Height

TESHL · rs1864440

See detailed info → Standard

Height

near RNA5SP112 · rs1529089

See detailed info → Standard

Height

DOCK9 · rs12429249

See detailed info → Standard

Height

SERPINA1 · rs1028580

See detailed info → Standard

Height

near LINC03080 · rs7165608

See detailed info → Standard

Height

near RSL24D1P1 · rs6901437

See detailed info → Standard

Height

NKIRAS1 · rs4131864

See detailed info →

Showing 20 of 10926 · page 153 of 547

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.