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

11,668 positions on this site are linked to Height, out of 2,512,045 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

USHBP1 · rs34084277

See detailed info → Standard

Height

LYPLAL1-DT · rs11118178

See detailed info → Standard

Height

NSD2 · rs10488835

See detailed info → Standard

Height

DDX27 · rs13038866

See detailed info → Standard

Height

TOX · rs7838499

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Height

MYO9B · rs2880937

See detailed info → Standard

Height

ADGRV1 · rs949789

See detailed info → Standard

Height

ARHGAP32 · rs590458

See detailed info → Standard

Height

PCGF5 · rs11186478

See detailed info → Standard

Height

SCAF11 · rs10880872

See detailed info → Standard

Height

PCSK5 · rs958225

See detailed info → Standard

Height

near KCNS3 · rs776

See detailed info → Standard

Height

PARPBP · rs17032311

See detailed info → Standard

Height

near TBX15 · rs2712252

See detailed info → Standard

Height

CFAP36 · rs17736300

See detailed info → Standard

Height

TDG · rs4135054

See detailed info → Standard

Height

LPAR1 · rs10980653

See detailed info → Standard

Height

BNIP1 · rs3805463

See detailed info → Standard

Height

CDC25A · rs3731563

See detailed info → Standard

Height

WWC2 · rs6852303

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Showing 20 of 11668 · page 47 of 584

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.