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 12, 2026

11,888 positions on this site are linked to Height, out of 2,516,151 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 GRM1 · rs863820

See detailed info →
Standard

Height

DNAAF10 · rs4078978

See detailed info →
Standard

Height

NUP205 · rs10224307

See detailed info →
Standard

Height

near GCH1 · rs17671345

See detailed info →
Standard

Height

near PRDX3 · rs10886416

See detailed info →
Standard

Height

near H2BC9 · rs3999543

See detailed info →
Standard

height (mean, inv-normal transformed)

near PRKG2 · rs3114140

See detailed info →
Standard

Height

MYEOV · rs12803098

See detailed info →
Standard

Height

RPL5 · rs11540832

See detailed info →
Standard

Height

DLC1 · rs2278945

See detailed info →
Standard

Height

BLTP3A · rs3734261

See detailed info →
Standard

Standing height (UKB data field 50)

near PXMP4 · rs548466113

See detailed info →
Standard

Height

near MTCO3P1 · rs3104404

See detailed info →
Standard

Height

near KRT18P9 · rs7744288

See detailed info →
Standard

Height

near MXD4 · rs762832

See detailed info →
Standard

Height

near CCDC91 · rs231210

See detailed info →
Standard

Height

near ZNF619P1 · rs13228308

See detailed info →
Standard

Height

HHIP · rs2575580

See detailed info →
Standard

Height

DKK3 · rs3206824

See detailed info →
Standard

Height

HDAC9 · rs13245206

See detailed info →

Showing 20 of 11888 · page 70 of 595

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.