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

11,159 positions on this site are linked to Height, out of 2,506,722 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

Height (baseline)

near CLXN · rs3750259

See detailed info → Standard

Height

UBR2 · rs3749898

See detailed info → Standard

Height

TCF19 · rs3734864

See detailed info → Standard

Height

ZNF785 · rs35974081

See detailed info → Standard

Height (baseline)

KPNA5 · rs35863134

See detailed info → Standard

Height (baseline)

near ITGB8 · rs34795179

See detailed info → Standard

Height (baseline)

IGF2BP3 · rs34607168

See detailed info → Standard

Height

DCN · rs3138276

See detailed info → Standard

Height

FGFR2 · rs3135715

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

near SPRY4 · rs2908536

See detailed info → Standard

Height

near DCUN1D4 · rs28875284

See detailed info → Standard

Height (baseline)

COP1-DT · rs2861745

See detailed info → Standard

Height

SRGAP3 · rs2700331

See detailed info → Standard

Height

near RPL37P6 · rs2609982

See detailed info → Standard

Height

near GJC3 · rs2571992

See detailed info → Standard

Height

FAM193B · rs2545802

See detailed info → Standard

Height (baseline)

HLA-F-AS1 · rs2523414

See detailed info → Standard

Height

near HIVEP3 · rs2492081

See detailed info → Standard

Height

near MYL6P5 · rs2429939

See detailed info → Standard

Height

near OSTN · rs2363957

See detailed info →

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.