Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 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 PPIF · rs181550583

See detailed info → Standard

Height (baseline)

FCSK · rs17884087

See detailed info → Standard

Height

TIAM2 · rs17736997

See detailed info → Standard

Height

BMP6 · rs17143141

See detailed info → Standard

Height

NLGN1 · rs16827431

See detailed info → Standard

Height (baseline)

MIDEAS · rs149195448

See detailed info → Standard

Height (baseline)

near ZFAT · rs146853256

See detailed info → Standard

Height

LRAT · rs146743395

See detailed info → Standard

Height (baseline)

CAMLG · rs144728507

See detailed info → Standard

Height

CSNK2A2 · rs144519609

See detailed info → Standard

Height (standard GWA)

PRKG2 · rs139545247

See detailed info → Standard

Height

near LINC01982 · rs1343951

See detailed info → Standard

Height

PDE5A · rs13103899

See detailed info → Standard

Height (standard GWA)

DCBLD2 · rs13083238

See detailed info → Standard

Height

near ZNF28 · rs12983988

See detailed info → Standard

Height

RASGRF1 · rs12911414

See detailed info → Standard

Height (baseline)

ZBTB18 · rs12027747

See detailed info → Standard

Height

HMGA2-AS1 · rs11834895

See detailed info → Standard

Height (baseline)

near MIR4465 · rs11757795

See detailed info → Standard

Height

MARK3 · rs11622835

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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.