Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,452 positions on this site are linked to Height, out of 2,509,202 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)

LINC00471 · rs111305583

See detailed info → Standard

Height (baseline)

LRTM1 · rs11130440

See detailed info → Standard

Height (baseline)

WASHC3 · rs11111138

See detailed info → Standard

Height

RSRC1 · rs1104288

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Height

near PLXDC2 · rs11011941

See detailed info → Standard

Height

CACNB2 · rs10828270

See detailed info → Standard

Height

SOAT1 · rs10753191

See detailed info → Standard

Height (standard GWA)

FGF2 · rs10518406

See detailed info → Standard

Height (standard GWA)

LINC03138 · rs9982634

See detailed info → Standard

Height (baseline)

VRK2 · rs966721

See detailed info → Standard

Height

EFNB2 · rs9555252

See detailed info → Standard

Height (baseline)

near MRPS21P6 · rs9423029

See detailed info → Standard

Height (baseline)

LINC02571 · rs9380239

See detailed info → Standard

Height (baseline)

ESR1 · rs9340874

See detailed info → Standard

Height (standard GWA)

BCAS3 · rs8073676

See detailed info → Standard

Height (baseline)

near RNU6-745P · rs8026461

See detailed info → Standard

Height (baseline)

LRP5 · rs7924398

See detailed info → Standard

Height (baseline)

UQCC1 · rs78319794

See detailed info → Standard

Height (baseline)

near RPL26P20 · rs78307876

See detailed info → Standard

Height (baseline)

TOX · rs7815388

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Showing 20 of 11452 · page 244 of 573

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.