Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 12, 2026

11,879 positions on this site are linked to Height, out of 2,515,865 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

MIR2052HG · rs1036266

See detailed info → Standard

Height

CHFR · rs10357

See detailed info → Standard

Height (baseline)

near PPIAP76 · rs1028197

See detailed info → Standard

Height

LINC02182 · rs1019560

See detailed info → Standard

Height

ARHGAP26 · rs10054462

See detailed info → Standard

Height

MAP3K4 · rs9458118

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Height

SEPTIN11 · rs878729

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Height (baseline)

MUC22 · rs7739491

See detailed info → Standard

Height (baseline)

CFAP299 · rs76928054

See detailed info → Standard

Height (standard GWA)

SSR1 · rs75892127

See detailed info → Standard

Height (baseline)

LINC01752 · rs73086186

See detailed info → Standard

Height (baseline)

CREBRF · rs72816131

See detailed info → Standard

Height

near RPS6P12 · rs7033356

See detailed info → Standard

Height

HDAC9 · rs6968715

See detailed info → Standard

Height

MECOM · rs6788901

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Height

near RNU6-500P · rs6556072

See detailed info → Standard

Height

SSBP3 · rs608386

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Height

PTP4A2 · rs601261

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Height (baseline)

near H2BC7 · rs557637621

See detailed info → Standard

Height (baseline)

near SMIM23 · rs537304226

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Showing 20 of 11879 · page 355 of 594

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.