Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,037 positions on this site are linked to Height, out of 2,506,010 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

near PRR29-AS1 · rs11653059

See detailed info →
Standard

Height

near PAQR8 · rs9370112

See detailed info →
Standard

Height

SLC39A14 · rs3943520

See detailed info →
Standard

Height

near SEMA3D · rs2732742

See detailed info →
Standard

Height

TPH1 · rs10488683

See detailed info →
Standard

Height

LINC02664 · rs793088

See detailed info →
Standard

Height

HIPK2 · rs7458885

See detailed info →
Standard

Height

near DIS3L2 · rs6725657

See detailed info →
Standard

Height

COL8A1 · rs17778253

See detailed info →
Standard

Height

CDK5RAP3 · rs17617010

See detailed info →
Standard

Height

near LINC01973 · rs17550443

See detailed info →
Standard

Height

near RASGEF1B · rs17005127

See detailed info →
Standard

Height

near PRKG2 · rs17005093

See detailed info →
Standard

Height

near LMX1A · rs1506954

See detailed info →
Standard

Height

near NR2F6 · rs13343494

See detailed info →
Standard

Height

ZBTB20-AS1 · rs13084997

See detailed info →
Standard

Height

PHF2 · rs7040568

See detailed info →
Standard

Height

ZSWIM5 · rs4233496

See detailed info →
Standard

Standing height (UKB data field 50)

LRP5 · rs2306862

See detailed info →
Standard

Height

near ABTB3 · rs11113431

See detailed info →

Showing 20 of 11037 · page 170 of 552

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.