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 10, 2026

11,507 positions on this site are linked to Height, out of 2,509,918 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

DYM · rs11659570

See detailed info → Standard

Height

AC005152.3 · rs116878242

See detailed info → Standard

Height

SUZ12P1 · rs113900126

See detailed info → Standard

Height

NDUFS3 · rs11605348

See detailed info → Standard

Height

FGFR4 · rs2011077

See detailed info → Standard

Height

EFEMP1 · rs58754091

See detailed info → Standard

Height

RP11-63E9.1 · rs13213884

See detailed info → Standard

Height

ACAN · rs35148461

See detailed info → Standard

Height

SLC35D2 · rs7020954

See detailed info → Standard

Height

FER1L4 · rs57545942

See detailed info → Standard

Height

BCL2L2 · rs3210043

See detailed info → Standard

Height

TCP11 · rs6934818

See detailed info → Standard

Height

SERPINH1 · rs659418

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Height

RP11-51F16.1 · rs11542436

See detailed info → Standard

Height

TRAF7 · rs2078282

See detailed info → Standard

Height

HMGA2 · rs12371967

See detailed info → Standard

Height

GDF5OS · rs137874109

See detailed info → Standard

Height

FOXP1 · rs7647190

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Height

FAM184B · rs2109045

See detailed info → Standard

Height

RP11-600F24.7 · rs75482283

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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.