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 11, 2026

11,645 positions on this site are linked to Height, out of 2,511,617 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

Height

PDXDC1 · rs2740

See detailed info → Standard

Height

PTPRG · rs7621604

See detailed info → Standard

Height

near KRT18P9 · rs7742369

See detailed info → Standard

Height

near SF3B4 · rs11205277

See detailed info → Standard

Height

SERPINH1 · rs668347

See detailed info → Standard

Height

CABLES1 · rs4369779

See detailed info → Standard

Height

near ADAMTS3 · rs7697556

See detailed info → Standard

Height

near HMGN1P19 · rs723149

See detailed info → Standard

Height

HMGA2 · rs1351394

See detailed info → Standard

Height

near FBXW11 · rs4868126

See detailed info → Standard

Height

L3MBTL3 · rs7740188

See detailed info → Standard

Height

near SALRNA1 · rs10483727

See detailed info → Standard

Height

HMGA2 · rs8756

See detailed info → Standard

Height

LINC02240 · rs7709555

See detailed info → Standard

Height

CUX1 · rs2906649

See detailed info → Standard

Height

near AXIN2 · rs11651467

See detailed info → Standard

Height

LINC02953 · rs10796817

See detailed info → Standard

Height (baseline)

LINC01556 · rs6914955

See detailed info → Standard

Height

near GALM-AS1 · rs10204680

See detailed info → Standard

Height

near TCOF1 · rs10044860

See detailed info →

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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.