Gene Knowledge Graph
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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.

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

← Back to Height

Standard

Standing height (UKB data field 50)

SMAD6 · rs6494597

See detailed info → Standard

Height

LINC02796 · rs4509530

See detailed info → Standard

Height

CAP2 · rs10949426

See detailed info → Standard

Height (baseline)

LTBP1 · rs963025

See detailed info → Standard

Height

ZBTB38 · rs6795398

See detailed info → Standard

Height

EIF2AK3-AS1 · rs6740205

See detailed info → Standard

Height

XRRA1 · rs3814726

See detailed info → Standard

Height

ZBTB20 · rs2669885

See detailed info → Standard

Height

near LINC02392 · rs12831322

See detailed info → Standard

Height

MIR493HG · rs11851174

See detailed info → Standard

Height

YAF2 · rs10880274

See detailed info → Standard

Height

LINC02898 · rs4952548

See detailed info → Standard

Height

near SYTL2 · rs4944539

See detailed info → Standard

Height

TBPL2 · rs17743484

See detailed info → Standard

Height

TEAD1 · rs12807395

See detailed info → Standard

Height

ERGIC1 · rs10213832

See detailed info → Standard

Height

near PRRX1 · rs6663331

See detailed info → Standard

Height

SNX29 · rs6498261

See detailed info → Standard

Height

near TBC1D22A-DT · rs5769136

See detailed info → Standard

Height

PDGFC · rs4691381

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Showing 20 of 10927 · page 158 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.