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 2,505,721 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

C6orf106 · rs2814993

See detailed info →
Standard

Height

GPR126 · rs3748069

See detailed info →
Standard

Sitting height ratio

NFATC2 · rs228836

See detailed info →
Standard

Height

EXTL3 · rs10448080

See detailed info →
Standard

Height

SLC17A2 · rs1865760

See detailed info →
Standard

Height

JMJD4 · rs10799445

See detailed info →
Standard

Height

CCDC108/IHH · rs12470505

See detailed info →
Standard

Height

TLE3 · rs10152591

See detailed info →
Standard

Height

ATP5SL · rs17318596

See detailed info →
Standard

Height

DIS3L2 · rs3103267

See detailed info →
Standard

Height

RDHE2 · rs4075154

See detailed info →
Standard

Height

LYPLAL1 · rs11118346

See detailed info →
Standard

Height

ADAM28 · rs1013209

See detailed info →
Standard

Height

PCCB · rs9844666

See detailed info →
Standard

Height

PEX2 · rs6473015

See detailed info →
Standard

Height

HLA locus · rs6457620

See detailed info →
Standard

Height

BOD1 · rs889014

See detailed info →
Standard

Height

OR2J3 · rs3129109

See detailed info →
Standard

Height

C3orf47 · rs6439167

See detailed info →
Standard

Height

IGF2BP3 · rs12534093

See detailed info →

Showing 20 of 10927 · page 543 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.