Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 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

near U6 · rs7677078

See detailed info → Standard

Height

SETD1B · rs2242259

See detailed info → Standard

Height

HMGA2 · rs1038196

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Height

NCOA6 · rs13044899

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Height

GATA3-AS1 · rs2275806

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Height

RCN1 · rs223046

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Height (maximum, inv-normal transformed)

MGMT · rs4751100

See detailed info → Standard

Height

BRD1 · rs4468

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Height

IGF2-AS · rs1003484

See detailed info → Standard

height (minimum, inv-normal transformed)

EVI5 · rs6603984

See detailed info → Standard

Height

DDAH1 · rs11161636

See detailed info → Standard

Height

near RNU7-167P · rs5750089

See detailed info → Standard

Height

RP11-513I15.6 · rs1759637

See detailed info → Standard

Height

GRB10 · rs2715094

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height (mean, inv-normal transformed)

WWP2 · rs11641521

See detailed info → Standard

Height

ZNF638 · rs4852777

See detailed info → Standard

height (minimum, inv-normal transformed)

near PSPHP1 · rs10232851

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Standing height (UKB data field 50)

PREX1 · rs2664521

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Height (maximum, inv-normal transformed)

EML4 · rs10200353

See detailed info → Standard

Height (baseline)

DGKH · rs9533031

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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.