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

11,879 positions on this site are linked to Height, out of 2,515,865 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

PTPRD · rs10977146

See detailed info → Standard

Height

GRB10 · rs10486759

See detailed info → Standard

Height

near LINC03020 · rs10108298

See detailed info → Standard

Height

near ITGA11 · rs1001605

See detailed info → Standard

Height

DOCK4 · rs970890

See detailed info → Standard

Height

near C8orf90 · rs903959

See detailed info → Standard

Height (baseline)

PTPRS · rs8100053

See detailed info → Standard

Height

CPLX4 · rs8098279

See detailed info → Standard

Height

near RGMA · rs8038806

See detailed info → Standard

Height (baseline)

VWA3B · rs80285452

See detailed info → Standard

Height

PRMT8 · rs7966000

See detailed info → Standard

Height (baseline)

near IL31RA · rs7728232

See detailed info → Standard

Height (baseline)

near AXIN2 · rs7406690

See detailed info → Standard

Height (baseline)

near LINC02950 · rs73499199

See detailed info → Standard

Height

near LINC02582 · rs6566728

See detailed info → Standard

Height

ELK3 · rs6538703

See detailed info → Standard

Height (baseline)

MIR493HG · rs45500403

See detailed info → Standard

Height (baseline)

ECI1 · rs34713291

See detailed info → Standard

Height

EXTL3 · rs2856802

See detailed info → Standard

Height

MRPS6 · rs2834455

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.