Gene Knowledge Graph
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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

11,295 positions on this site are linked to Height, out of 2,507,931 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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

← Back to Height

Standard

Height

SLC35D2 · rs7020954

See detailed info → Standard

Height

RP11-63E9.1 · rs13213884

See detailed info → Standard

Height

FAM184B · rs2109045

See detailed info → Standard

Height

HMGA2 · rs55981861

See detailed info → Standard

Height

JAZF1 · rs73091214

See detailed info → Standard

Height

FOXP1 · rs7647190

See detailed info → Standard

Height

RP11-600F24.7 · rs75482283

See detailed info → Standard

Height

PLAG1 · rs62515432

See detailed info → Standard

Height

GDF5OS · rs137874109

See detailed info → Standard

Height

HMGA2 · rs12371967

See detailed info → Standard

Height

RP11-51F16.1 · rs11542436

See detailed info → Standard

Height

TRAF7 · rs2078282

See detailed info → Standard

Height

SERPINH1 · rs659418

See detailed info → Standard

Height

RPS26P45 · rs10878984

See detailed info → Standard

Height

C6orf106 · rs2814973

See detailed info → Standard

Height

FAM83C · rs6060347

See detailed info → Standard

Height

PXYLP1 · rs28721484

See detailed info → Standard

Height

DIS3L2 · rs111551994

See detailed info → Standard

Height

RNY5 · rs80085026

See detailed info → Standard

Height

ADAP2 · rs35958868

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Showing 20 of 11295 · page 552 of 565

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.