Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,659 positions on this site are linked to Height, out of 2,511,894 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

CASC17 · rs6501447

See detailed info → Standard

Height

near RN7SL366P · rs9295227

See detailed info → Standard

Height

SCUBE1 · rs139027

See detailed info → Standard

Height

near DAAM2 · rs9471165

See detailed info → Standard

Height

TP53 · rs17884512

See detailed info → Standard

Height

ITPK1 · rs17128721

See detailed info → Standard

Height

near GAPDHP31 · rs11054376

See detailed info → Standard

Height

CTBP2 · rs10794201

See detailed info → Standard

Height

NNT · rs7702621

See detailed info → Standard

Height

SLC35D2 · rs13283885

See detailed info → Standard

Height

NPR3 · rs1458053

See detailed info → Standard

Height

near SRC · rs6017901

See detailed info → Standard

Height

LHPP · rs11599744

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Height

near PNMA8A · rs8108405

See detailed info → Standard

Height

ARHGAP12 · rs7077016

See detailed info → Standard

Height

FBXW11 · rs17569783

See detailed info → Standard

Height

near ARHGEF28P1 · rs7631745

See detailed info → Standard

Height

CACNA2D3 · rs358498

See detailed info → Standard

Height

ABCB5 · rs12154301

See detailed info → Standard

Height (baseline)

DLEU1 · rs2703083

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Showing 20 of 11659 · page 40 of 583

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.