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

11,639 positions on this site are linked to Height, out of 2,511,480 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

BAIAP2 · rs4075483

See detailed info → Standard

Height

NUDT6 · rs12648093

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Height

near CHSY1 · rs7175522

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Height

CRADD · rs3858603

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Height

near ERGIC2 · rs2278093

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Height

GNA12 · rs798490

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Height

near SMAD7 · rs12968652

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Height

near LINC02747 · rs2002028

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Height

near FRYL · rs10031777

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Height

near FBN1-DT · rs8042197

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Height

DOCK3 · rs13088462

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Height

FUBP3 · rs11791149

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Height

WWP2 · rs3790085

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Height

WWC2 · rs955748

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Height

WBP1L · rs12763284

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Height

near STARD3NL · rs6963134

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Height

BOK · rs4675801

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Height

HELLPAR · rs7313075

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Height

near CASC20 · rs967417

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Height

near TET2 · rs7661349

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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.