Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,468 positions on this site are linked to Height, out of 2,509,439 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 RNA5SP45 · rs34125970

See detailed info → Standard

Height

near SEMA3C · rs327674

See detailed info → Standard

Height (standard GWA)

ETV6 · rs3020924

See detailed info → Standard

Height

TG · rs2979040

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Height

PRDM9 · rs2914263

See detailed info → Standard

Height

SH3PXD2B · rs2879468

See detailed info → Standard

Height

KCNE1 · rs2834489

See detailed info → Standard

Height

LNPEP · rs27997

See detailed info → Standard

Height

CR1L · rs2761424

See detailed info → Standard

Height (standard GWA)

C4orf17 · rs2718687

See detailed info → Standard

Height

near FOXCUT · rs2569839

See detailed info → Standard

Height (baseline)

PDPN · rs2487628

See detailed info → Standard

Height

AGRN · rs2465136

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Height

near MIR1275 · rs2451374

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Height

near Y_RNA · rs2431664

See detailed info → Standard

Height

KIAA0753 · rs2304977

See detailed info → Standard

Height (baseline)

SLC4A2 · rs2303930

See detailed info → Standard

Height

PIEZO2 · rs2298745

See detailed info → Standard

Height (baseline)

near CELF2-DT · rs2265023

See detailed info → Standard

Height (baseline)

PCNX4-DT · rs219387

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Showing 20 of 11468 · page 260 of 574

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.