Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,493 positions on this site are linked to Height, out of 2,509,702 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)

BCAS3 · rs189634497

See detailed info → Standard

Height (baseline)

near HLA-DRB5 · rs189189739

See detailed info → Standard

Height (baseline)

HOXB7 · rs186639828

See detailed info → Standard

Height

SEMA6D · rs1865647

See detailed info → Standard

Height

near NFATC1 · rs183374

See detailed info → Standard

Height (baseline)

PPARA · rs1800206

See detailed info → Standard

Height

CNDP2 · rs17816304

See detailed info → Standard

Height

near ADAM24P · rs17632120

See detailed info → Standard

Height

LINC03090 · rs17381988

See detailed info → Standard

Height

NFIA · rs17375290

See detailed info → Standard

Height (baseline)

MIR217HG · rs17279566

See detailed info → Standard

Height

HAND2-AS1 · rs17263985

See detailed info → Standard

Height

SUGCT · rs17171704

See detailed info → Standard

Height

near RNU6-508P · rs17050288

See detailed info → Standard

Height (baseline)

SOCS2 · rs17021323

See detailed info → Standard

Height

CDC42EP3-AS1 · rs17021120

See detailed info → Standard

Height

PAK3 · rs16986436

See detailed info → Standard

Height

C8orf34 · rs16935095

See detailed info → Standard

Height

near RN7SKP135 · rs16930513

See detailed info → Standard

Height

near UBE2V1P14 · rs16857132

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Showing 20 of 11493 · page 304 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.