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

10,927 positions on this site are linked to Height, out of 2,505,673 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 ALX4 · rs6485513

See detailed info →
Standard

Height

PTPRM · rs6506523

See detailed info →
Standard

Height

near PDE5A · rs6534157

See detailed info →
Standard

Height

near BDH1 · rs6583209

See detailed info →
Standard

Height

SP3 · rs66770364

See detailed info →
Standard

Height

GAREM1 · rs67874253

See detailed info →
Standard

Height

near BEND4 · rs6819984

See detailed info →
Standard

Height

DNAAF4 · rs7175171

See detailed info →
Standard

Height

STX8 · rs72814125

See detailed info →
Standard

Height

VAMP5 · rs72843872

See detailed info →
Standard

Height

near ABCB1 · rs73198349

See detailed info →
Standard

Height

near SMNDC1 · rs73358755

See detailed info →
Standard

Height

DENND6B · rs73439331

See detailed info →
Standard

Height

near LNX2 · rs77393241

See detailed info →
Standard

Height

PAN3 · rs77632592

See detailed info →
Standard

Height

PDGFC · rs78256087

See detailed info →
Standard

Height

ZNF516 · rs78380260

See detailed info →
Standard

Height

MGMT · rs7911018

See detailed info →
Standard

Height

near MMS22L · rs9400761

See detailed info →
Standard

Height x sex interaction

CYP19A1 · rs730154

See detailed info →

Showing 20 of 10927 · page 539 of 547

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.