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

11,375 positions on this site are linked to Height, out of 2,508,530 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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

← Back to Height

Height (baseline)

LINC02603 · rs146618080

See detailed info → Standard

Height

ARHGEF38 · rs1374530

See detailed info → Standard

Height

near MIR4733HG · rs12939322

See detailed info → Standard

Height

ME3 · rs12804208

See detailed info → Standard

Height

near HLA-DRB1 · rs11754183

See detailed info → Standard

Height

near TEX29 · rs11619721

See detailed info → Standard

Height

near LINC01808 · rs1095014

See detailed info → Standard

Height

CAST · rs10055259

See detailed info → Standard

Height

THRB · rs9870108

See detailed info → Standard

Height

ZNF496 · rs9725334

See detailed info → Standard

Height

ABCC8 · rs7950189

See detailed info → Standard

Height

near CAMK2B · rs7797038

See detailed info → Standard

Standing height (UKB data field 50)

MICA-AS1 · rs73398306

See detailed info → Standard

Height (baseline)

near RNA5SP56 · rs72701494

See detailed info → Standard

Height

ESR1 · rs6939257

See detailed info → Standard

Height (baseline)

HIVEP2 · rs638880

See detailed info → Standard

Height

RANBP17 · rs4593283

See detailed info → Standard

Height

DYNC1I1 · rs2299293

See detailed info → Standard

Height (baseline)

NF1 · rs17884401

See detailed info → Standard

Height

L3MBTL3 · rs1572292

See detailed info →

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.