Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,351 positions on this site are linked to Height, out of 2,508,348 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 LINC01982 · rs1343951

See detailed info → Standard

Height

PDE5A · rs13103899

See detailed info → Standard

Height (standard GWA)

DCBLD2 · rs13083238

See detailed info → Standard

Height

near ZNF28 · rs12983988

See detailed info → Standard

Height

RASGRF1 · rs12911414

See detailed info → Standard

Height (baseline)

ZBTB18 · rs12027747

See detailed info → Standard

Height

HMGA2-AS1 · rs11834895

See detailed info → Standard

Height (baseline)

near MIR4465 · rs11757795

See detailed info → Standard

Height

MARK3 · rs11622835

See detailed info → Standard

Height (baseline)

near CCDC12 · rs114404763

See detailed info → Standard

Height

GPR135 · rs113239787

See detailed info → Standard

Height

CS · rs11171792

See detailed info → Standard

Height

CCBE1 · rs11152156

See detailed info → Standard

Height

ABI1 · rs10829061

See detailed info → Standard

Height (standard GWA)

near ALDH7A1P4 · rs10822054

See detailed info → Standard

Height (standard GWA)

near MRPL42 · rs10777513

See detailed info → Standard

Height

FKBP9 · rs10266139

See detailed info → Standard

Height (baseline)

near RN7SKP277 · rs10240344

See detailed info → Standard

Height (standard GWA)

AMZ2 · rs9944517

See detailed info → Standard

Height

LINC00870 · rs9917816

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Showing 20 of 11351 · page 236 of 568

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.