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 12, 2026

11,888 positions on this site are linked to Height, out of 2,516,056 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

MEF2C-AS1 · rs1427970

See detailed info → Standard

Height

EFL1P1 · rs12911210

See detailed info → Standard

Height

IGF2BP3 · rs12533936

See detailed info → Standard

Height

near RN7SKP208 · rs11900078

See detailed info → Standard

Height

CCDC91 · rs11049620

See detailed info → Standard

Height

ITGB8 · rs10256769

See detailed info → Standard

Height

CABLES1 · rs11875837

See detailed info → Standard

Height

FNDC3B · rs12637941

See detailed info → Standard

Height

near DLX5 · rs1207726

See detailed info → Standard

Height

NPFFR1 · rs3812694

See detailed info → Standard

Height (baseline)

near TBC1D29P · rs112707384

See detailed info → Standard

Height

MSI2 · rs703862

See detailed info → Standard

Height

CFAP61 · rs2424340

See detailed info → Standard

Height

SPPL3 · rs514108

See detailed info → Standard

Height

LINC02742 · rs7126178

See detailed info → Standard

Height

DICER1 · rs1057035

See detailed info → Standard

Height

BCL6B · rs10521149

See detailed info → Standard

Height

SLC6A12 · rs495360

See detailed info → Standard

Height (baseline)

ITGB8 · rs3807945

See detailed info → Standard

Height

near LINC02160 · rs1479644

See detailed info →

Showing 20 of 11888 · page 64 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.