Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,348 positions on this site are linked to Height, out of 107,684 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Height

Standard

Height (baseline)

near RNA5SP214 · rs145833963

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Standard

Height (standard GWA)

FILIP1 · rs145206747

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Standard

Height (baseline)

near RPL34-DT · rs141852021

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Standard

Height (baseline)

WDR70 · rs141467459

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Standard

Height (baseline)

ITSN2 · rs141370798

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Standard

Height

near MYBL1 · rs140121875

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Standard

Height (standard GWA)

CCDC91 · rs139958466

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Standard

Height

DLC1 · rs1383942

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Standard

Height

near NRN1 · rs13210587

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Standard

Height

RORA · rs1318929

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Standard

Height (baseline)

LINC01418 · rs12909073

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Standard

Height (baseline)

MECOM · rs1273882

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Standard

Height

near C6orf118 · rs12528341

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Standard

Height

CTNNA3 · rs12355064

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Standard

Height

near DDX10P2 · rs12344716

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Standard

Height

PCAT1 · rs12334903

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Standard

Height

near LINC01871 · rs12105768

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Standard

Height

FGF10 · rs11750845

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Standard

Height (baseline)

CRADD · rs117489926

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Standard

Height (baseline)

DNAJC3 · rs117402539

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Showing 20 of 9348 · page 16 of 468

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.