Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,193 positions on this site are linked to Height, out of 106,172 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

CACNA1D · rs12053905

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Standard

Height

near SEC63P2 · rs11732820

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Standard

Height (baseline)

near RPL23AP12 · rs117160808

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Standard

Height (baseline)

SPDEF · rs115655366

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Standard

Height (baseline)

near ANAPC13 · rs114432254

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Standard

Height

RPL17P50 · rs113905969

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Standard

Height

near ARL4A · rs10950409

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Standard

Height

ENOX1 · rs1044753

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Standard

Height

LINC01505 · rs10115173

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Standard

Height (baseline)

near LINC00917 · rs9923266

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Standard

Height

CAST · rs9918149

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Standard

Height

PPARD · rs9658118

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Standard

Height

near RNU6-669P · rs9409567

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Standard

Height

EFCAB6-DT · rs8138497

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Standard

Height

LINC02464 · rs7968353

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Standard

Height (baseline)

GPR149 · rs789298

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Standard

Height (baseline)

NCOA1 · rs78500502

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Standard

Height (baseline)

near Y_RNA · rs78331472

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Standard

Height

near INHBA-AS1 · rs7805201

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Standard

Height (baseline)

near GUSBP5 · rs77887721

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Showing 20 of 9193 · page 1 of 460

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.