Gene Knowledge Graph
UTC

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

10,926 positions on this site are linked to Height, out of 2,505,576 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Clear
Recommended (connected, strongest) Strongest evidence Newest Oldest

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

← Back to Height

Standard

Height

PLOD2 · rs34901222

See detailed info → Standard

Height

ZZEF1 · rs12938597

See detailed info → Standard

Height

MKLN1 · rs12112721

See detailed info → Standard

Height

near RPS26P38 · rs10887732

See detailed info → Standard

Height

KCNE4 · rs10172933

See detailed info → Standard

Height

CTDSPL · rs9822761

See detailed info → Standard

Height

near NXNP1 · rs6541219

See detailed info → Standard

Height

GSE1 · rs4783146

See detailed info → Standard

Height

near EFL1P1 · rs4420497

See detailed info → Standard

Height

ABR · rs17623512

See detailed info → Standard

Height

near SNHG26 · rs12535331

See detailed info → Standard

Height

near HMGB3P18 · rs11752019

See detailed info → Standard

Height

RFX2-AS2 · rs7256341

See detailed info → Standard

Height

near PDGFRA · rs6554162

See detailed info → Standard

Height (baseline)

SPI1 · rs4752987

See detailed info → Standard

Height

LINC02255 · rs4555110

See detailed info → Standard

Height

PELI2 · rs242413

See detailed info → Standard

Height

AP2A2 · rs11605562

See detailed info → Standard

Height

near LRRC10 · rs11177752

See detailed info → Standard

Height

BEND4 · rs4132888

See detailed info →

Showing 20 of 10926 · page 154 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.