Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,351 positions on this site are linked to Height, out of 2,508,348 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

FAM20C · rs28644307

See detailed info → Standard

Height (standard GWA)

UBE3D · rs2770675

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Height

AHCYL2 · rs2718096

See detailed info → Standard

Height (baseline)

PRKG1 · rs2666543

See detailed info → Standard

Height (standard GWA)

near ARHGAP26 · rs258755

See detailed info → Standard

Height (baseline)

NINJ2 · rs2240893

See detailed info → Standard

Height (baseline)

LINC01755 · rs1963328

See detailed info → Standard

Height (standard GWA)

LINC01621 · rs1960739

See detailed info → Standard

Height

LINC01725 · rs187084421

See detailed info → 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

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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

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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.