Gene Knowledge Graph

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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,452 positions on this site are linked to Height, out of 2,509,202 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)

DNM3 · rs17369123

See detailed info → Standard

Height

EFEMP1 · rs35387878

See detailed info → Standard

Height (baseline)

near RPSAP72 · rs564286779

See detailed info → Standard

Height (baseline)

SNAI1 · rs4647959

See detailed info → Standard

Height (baseline)

PLPP1 · rs34802366

See detailed info → Standard

Height

near GPR139 · rs2521478

See detailed info → Standard

Height

near FAM120B · rs11755081

See detailed info → Standard

Height (baseline)

near PTCH1 · rs113343136

See detailed info → Standard

Height

GLDC · rs4742213

See detailed info → Standard

Height (baseline)

GUSBP5 · rs17017911

See detailed info → Standard

Height

ATG101 · rs7138000

See detailed info → Standard

Height (baseline)

OTUD7B · rs61807555

See detailed info → Standard

Height

ARHGEF12 · rs12785387

See detailed info → Standard

Height (baseline)

near HHIP · rs13127923

See detailed info → Standard

Standing height (UKB data field 50)

near BSX · rs10892940

See detailed info → Standard

Height

DDX23 · rs1057908

See detailed info → Standard

Height

near MIR375 · rs371825

See detailed info → Standard

Height

near RPL23AP75 · rs1009570

See detailed info → Standard

Height

LNCAROD · rs6480933

See detailed info → Standard

Height (baseline)

near RPS4XP9 · rs9375460

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.