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 6, 2026

10,753 positions on this site are linked to Height, out of 2,500,639 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

BMP6 · rs1885486

See detailed info →
Standard

Height

MYO9A · rs12902421

See detailed info →
Standard

Height

STAT2 · rs2066807

See detailed info →
Standard

Height

SENP6 · rs9360921

See detailed info →
Standard

Height

FER · rs13177718

See detailed info →
Standard

Height

C2orf52 · rs6750795

See detailed info →
Standard

Height

PPARD/FANCE · rs6457821

See detailed info →
Standard

Height

IPPK · rs9969804

See detailed info →
Standard

Height

DNAJC27 · rs4665736

See detailed info →
Standard

Height

NUCB2 · rs1330

See detailed info →
Standard

Height

SLBP/FGFR3 · rs2247341

See detailed info →
Standard

Height

LIN28 · rs7532866

See detailed info →
Standard

Height

DTL · rs10863936

See detailed info →
Standard

Height

TEAD1 · rs7926971

See detailed info →
Standard

Height

RHOD · rs7112925

See detailed info →
Standard

Height

TREH · rs494459

See detailed info →
Standard

Height

PAPPA2 · rs1325598

See detailed info →
Standard

Height

C2orf34 · rs2341459

See detailed info →
Standard

Height

MYO9B · rs2279008

See detailed info →
Standard

Height

LRRC37B · rs17780086

See detailed info →

Showing 20 of 10753 · page 537 of 538

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.