Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,487 positions on this site are linked to Height, out of 2,509,560 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)

near NVL · rs74536714

See detailed info → Standard

Height (baseline)

ABCB9 · rs73230017

See detailed info → Standard

Height (baseline)

HMGA2-AS1 · rs73119896

See detailed info → Standard

Height

RBFOX1 · rs713115

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Height (baseline)

EED · rs7120070

See detailed info → Standard

Height (standard GWA)

CCDC26 · rs7011623

See detailed info → Standard

Height

HCN1 · rs6874127

See detailed info → Standard

Height

near MIR4433B · rs67968328

See detailed info → Standard

Height (baseline)

near COL8A1 · rs6765040

See detailed info → Standard

Height

near VMA22 · rs6708453

See detailed info → Standard

Height

LINC00595 · rs6480895

See detailed info → Standard

Height (baseline)

CHCHD7 · rs6474051

See detailed info → Standard

Height

near PARP11-AS1 · rs638977

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Height

FLI1 · rs609017

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Height (baseline)

near LINC01428 · rs6077123

See detailed info → Standard

Height (baseline)

TAS1R1 · rs57065667

See detailed info → Standard

Height (baseline)

GRM5P1 · rs567540722

See detailed info → Standard

Height (standard GWA)

FNDC3B · rs56365527

See detailed info → Standard

Height (baseline)

LRRK1-AS1 · rs548584289

See detailed info → Standard

Height (baseline)

DNAH2 · rs533443079

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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.