Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,129 positions on this site are linked to Height, out of 2,506,622 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

SDR16C5 · rs7460090

See detailed info → Standard

Height

DNM3 · rs17346452

See detailed info → Standard

Height

CDK6 · rs42235

See detailed info → Standard

Height

PTCH1/FANCC · rs473902

See detailed info → Standard

Height

PDS5B/BRCA2 · rs7332115

See detailed info → Standard

Height

QSOX2 · rs7849585

See detailed info → Standard

Height

EIF2AK3 · rs11684404

See detailed info → Standard

Height

PRKG2/BMP3 · rs788867

See detailed info → Standard

Height

CCDC53/GNPTAB · rs7971536

See detailed info → Standard

Height

ZBTB38 · rs6440003

See detailed info → Standard

Height

LCORL · rs7678436

See detailed info → Standard

Height

ZBTB38 · rs9825379

See detailed info → Standard

Height

DIS3L2 · rs7571816

See detailed info → Standard

Height

HMGA1 · rs6918981

See detailed info → Standard

Height

PLAG1 · rs13273123

See detailed info → Standard

Height

ZRANB3 · rs1900741

See detailed info → Standard

Height

RFC1 · rs2066789

See detailed info → Standard

Height

NEPRO-AS1 · rs1903431

See detailed info → Standard

Height

TMEM229B · rs8019974

See detailed info → Standard

Height

GNA12 · rs2266925

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Showing 20 of 11129 · page 213 of 557

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.