Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,344 positions on this site are linked to Height, out of 2,508,301 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

PTPRJ/SLC39A13 · rs10838801

See detailed info → Standard

Height

SCMH1 · rs2154319

See detailed info → Standard

Height

BNC2 · rs1319424

See detailed info → Standard

Height

ZMIZ1 · rs1815314

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Height (maximum, inv-normal transformed)

SRBD1 · rs17033679

See detailed info → Standard

Height

near TRPM8 · rs4663983

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Height

POGK · rs2272792

See detailed info → Standard

height (minimum, inv-normal transformed)

LINC00881 · rs12495519

See detailed info → Standard

Height

C3orf49 · rs832187

See detailed info → Standard

Height

KIZ · rs2252720

See detailed info → Standard

Height

ARID5B · rs4245597

See detailed info → Standard

Height

near LINC02058 · rs34509

See detailed info → Standard

height (mean, inv-normal transformed)

CREBRF · rs3095844

See detailed info → Standard

height (minimum, inv-normal transformed)

NFIC · rs55805295

See detailed info → Standard

Height

EPAS1 · rs4953353

See detailed info → Standard

Height

near GRP · rs7230581

See detailed info → Standard

Height

EHD3 · rs649729

See detailed info → Standard

Height

COLGALT2 · rs114661926

See detailed info → Standard

Height

HES7 · rs8067165

See detailed info → Standard

Height

H1-10-AS1 · rs4073154

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Showing 20 of 11344 · page 231 of 568

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.