Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,272 positions on this site are linked to Height, out of 2,507,630 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

OSBPL10 · rs12632849

See detailed info → Standard

Height

ALPL · rs1256348

See detailed info → Standard

Height

CD72 · rs12376747

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Height

near FCAMR · rs12066378

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Height

LINC00261 · rs1203870

See detailed info → Standard

Height (baseline)

near METTL27 · rs11772456

See detailed info → Standard

Height (baseline)

near DIDO1 · rs117411012

See detailed info → Standard

Height (baseline)

near RHPN1 · rs116803273

See detailed info → Standard

Height (baseline)

PFKFB4 · rs115671887

See detailed info → Standard

Height

near FGF3 · rs11263622

See detailed info → Standard

Height (baseline)

near PTPRJ · rs112132584

See detailed info → Standard

Height

FOXK2 · rs10852797

See detailed info → Standard

Height (baseline)

SLC8A3 · rs1035717

See detailed info → Standard

Height

CATSPERB · rs10162491

See detailed info → Standard

Height

BNC2 · rs10116407

See detailed info → Standard

Height (baseline)

IL31RA · rs10055201

See detailed info → Standard

Height

BMP2 · rs1005464

See detailed info → Standard

Height (baseline)

MLLT6 · rs9909435

See detailed info → Standard

Height

DOCK3 · rs9817077

See detailed info → Standard

Height

CRISPLD2 · rs965984074

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Showing 20 of 11272 · page 372 of 564

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.