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 9, 2026

11,335 positions on this site are linked to Height, out of 2,508,158 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

LINC01234 · rs11066633

See detailed info → Standard

Height

JMJD1C · rs10509186

See detailed info → Standard

Height

near CLPTM1 · rs10413089

See detailed info → Standard

Height

KANK1 · rs10156623

See detailed info → Standard

Height (baseline)

near ARL2BPP4 · rs10073435

See detailed info → Standard

Height

ASTN2 · rs7856625

See detailed info → Standard

Height

PIP4K2A · rs7099314

See detailed info → Standard

Height

SPRY4-AS1 · rs10515514

See detailed info → Standard

Height (baseline)

CADM4 · rs10402946

See detailed info → Standard

Height

SCAF4 · rs8132845

See detailed info → Standard

Height

near LINC02040 · rs56309511

See detailed info → Standard

Height

near KIF4B · rs190087249

See detailed info → Standard

Height

near TENT5A · rs12524255

See detailed info → Standard

Height decline (residual change score)

near LINC01894 · rs12455050

See detailed info → Standard

Height

GPR137B · rs7543562

See detailed info → Standard

Height (baseline)

TCF20 · rs62240933

See detailed info → Standard

Height (baseline)

DTNB · rs62130084

See detailed info → Standard

Height

BCL2L1-AS1 · rs6088962

See detailed info → Standard

Height

near STAU1 · rs3795075

See detailed info → Standard

Height

RERE · rs11121221

See detailed info →

Showing 20 of 11335 · page 526 of 567

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.