Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,491 positions on this site are linked to Height, out of 2,509,608 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 (baseline)

WDR70 · rs141467459

See detailed info → Standard

Height (baseline)

ITSN2 · rs141370798

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Height

near MYBL1 · rs140121875

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Height (standard GWA)

CCDC91 · rs139958466

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Height

DLC1 · rs1383942

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Height

near NRN1 · rs13210587

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Height

RORA · rs1318929

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Height (baseline)

LINC01418 · rs12909073

See detailed info → Standard

Height (baseline)

MECOM · rs1273882

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Height

near C6orf118 · rs12528341

See detailed info → Standard

Height

CTNNA3 · rs12355064

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Height

near DDX10P2 · rs12344716

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Height

PCAT1 · rs12334903

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Height

near LINC01871 · rs12105768

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Height

FGF10 · rs11750845

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Height (baseline)

CRADD · rs117489926

See detailed info → Standard

Height (baseline)

DNAJC3 · rs117402539

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Height

HHIP · rs117072351

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Height (baseline)

TGFBR3 · rs115401860

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Height (baseline)

near KLHL22 · rs1153427

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Showing 20 of 11491 · page 294 of 575

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.