Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,206 positions on this site are linked to Height, out of 2,507,095 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

CLEC3A · rs2072663

See detailed info → Standard

Height (baseline)

TRPC4AP · rs117046905

See detailed info → Standard

Height

PAPPA2 · rs1014719

See detailed info → Standard

Height

LEF1 · rs956237

See detailed info → Standard

Height (standard GWA)

GNA12 · rs1636248

See detailed info → Standard

Height

near CBX8 · rs12946718

See detailed info → Standard

Standing height (UKB data field 50)

near RNU2-36P · rs9410916

See detailed info → Standard

Height

PREX1 · rs729663

See detailed info → Standard

Height

WDR1 · rs11727087

See detailed info → Standard

Height

near RPL34-DT · rs56011514

See detailed info → Standard

Height

near PARLP2 · rs2216917

See detailed info → Standard

Height

near RPL13AP13 · rs1007984

See detailed info → Standard

Height

CRISPLD2 · rs4782673

See detailed info → Standard

Height

SPRY4-AS1 · rs253438

See detailed info → Standard

Height

near LINC01539 · rs10782046

See detailed info → Standard

Height

HAGHL · rs1406814

See detailed info → Standard

Height

ITPKC · rs2561530

See detailed info → Standard

Height

TLN2 · rs11635027

See detailed info → Standard

Height

C6orf173 · rs1155939

See detailed info → Standard

Height

LPP · rs3915010

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Showing 20 of 11206 · page 560 of 561

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.