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.

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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 (baseline)

ATE1 · rs117933296

See detailed info → Standard

Height (baseline)

DYM · rs117898212

See detailed info → Standard

Height

HDAC9 · rs1178111

See detailed info → Standard

Height

PLEC · rs11778018

See detailed info → Standard

Height (baseline)

CDK5RAP2 · rs117668013

See detailed info → Standard

Height

DAAM2 · rs11755202

See detailed info → Standard

Height (standard GWA)

WIPF2 · rs117447160

See detailed info → Standard

Height (baseline)

DPF3 · rs117136239

See detailed info → Standard

Height (baseline)

PUS10 · rs11682126

See detailed info → Standard

Height (baseline)

near POLRMTP1 · rs11656174

See detailed info → Standard

Height

FAM20A · rs11649965

See detailed info → Standard

Height (baseline)

CDC14A · rs11577884

See detailed info → Standard

Height (standard GWA)

LCORL · rs115218645

See detailed info → Standard

Height (standard GWA)

near GASK1A · rs114711402

See detailed info → Standard

Height (baseline)

ATP23 · rs113580822

See detailed info → Standard

Height (baseline)

ASTN1 · rs113536511

See detailed info → Standard

Height (baseline)

near RN7SL26P · rs113243085

See detailed info → Standard

Height (baseline)

LINC00924 · rs113080593

See detailed info → Standard

Height

SIK3 · rs11216162

See detailed info → Standard

Height (baseline)

NLN · rs112089614

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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.