Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,486 positions on this site are linked to Height, out of 2,509,513 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 LYPLAL1-AS1 · rs12091485

See detailed info → Standard

Height

near ASS1 · rs11790031

See detailed info → Standard

Height (baseline)

EPB41L1 · rs11697873

See detailed info → Standard

Height (baseline)

LMF1 · rs116928895

See detailed info → Standard

Height (baseline)

MEG8 · rs11628379

See detailed info → Standard

Height (baseline)

near U6 · rs115217914

See detailed info → Standard

Height (baseline)

near MTND5P34 · rs111437248

See detailed info → Standard

Height

near RPS27AP14 · rs10960642

See detailed info → Standard

Height (baseline)

near HLA-DQB2 · rs9461808

See detailed info → Standard

Height

near FAM241B · rs899021

See detailed info → Standard

Height (standard GWA)

LINC01080 · rs7990503

See detailed info → Standard

Height

CHST11 · rs7972699

See detailed info → Standard

Height (baseline)

PLAG1 · rs78470252

See detailed info → Standard

Height

DNM1 · rs78156728

See detailed info → Standard

Height (standard GWA)

near U6 · rs76872088

See detailed info → Standard

Height (baseline)

CXCR5 · rs76457018

See detailed info → Standard

Height (baseline)

DLK1 · rs75741145

See detailed info → Standard

Height (baseline)

TPCN2 · rs74674490

See detailed info → Standard

Height

TSPAN9 · rs740777

See detailed info → Standard

Height (baseline)

KIAA2012-AS1 · rs72936629

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Showing 20 of 11486 · page 280 of 575

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.