Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,928 positions on this site are linked to Height, out of 113,994 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

near UCK2 · rs16852868

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Standard

Height

LLGL2 · rs1671022

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Standard

Height (baseline)

DCTN2 · rs1669297

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Standard

Height

TRPM3 · rs1558926

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Standard

Height (baseline)

ANAPC10 · rs149685269

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Standard

Height (baseline)

near COL9A2 · rs149084861

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Standard

Height

BCKDHB · rs145101575

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Standard

Height (baseline)

PPARD · rs143853683

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Standard

Height (baseline)

near MOS · rs142856921

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Standard

Height

LINC01182 · rs1426126

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Standard

Height (baseline)

near SOCS2 · rs142519563

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Standard

Height (baseline)

near CD3E · rs141752759

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Standard

Height (baseline)

ADAMTSL3 · rs139578288

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Standard

Height (baseline)

near TMED7 · rs139443511

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Standard

Height

near Y_RNA · rs1389325

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Standard

Height (baseline)

near RN7SL316P · rs138044297

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Standard

Height (baseline)

near HCAR1 · rs137929115

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Standard

Height

PTPRK · rs1341597

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Standard

Height

DIS3L2 · rs13412942

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Height (baseline)

CSNK1G3 · rs13190325

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Showing 20 of 9928 · page 75 of 497

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.