Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,402 positions on this site are linked to Height, out of 108,284 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

ARHGEF11 · rs1572407

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Standard

Height (baseline)

UHRF1 · rs149372897

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Standard

Height (baseline)

JADE2 · rs148394728

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Standard

Height (baseline)

near RFX4 · rs147402868

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Standard

Height

MYO6 · rs1467462

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Standard

Height (baseline)

near KCNH2 · rs144563033

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Standard

Height (baseline)

near SLC38A6 · rs144203612

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Standard

Height (baseline)

SUGP2 · rs140411225

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Standard

Height (baseline)

ARMH3 · rs139965762

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Standard

Height

CA10 · rs1392934

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Standard

Height (baseline)

GMDS-DT · rs138556004

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Standard

Height

near RFX3-DT · rs13296612

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Standard

Height

ADAMTSL2 · rs13288485

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Standard

Height

SFMBT1 · rs1328122506

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Standard

Height

SEMA3A · rs12673519

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Standard

Height (baseline)

near Metazoa_SRP · rs12592780

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Standard

Height

near TENM3-AS1 · rs12508055

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Standard

Height (baseline)

SP3 · rs12477091

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Standard

Height (baseline)

TGFB2 · rs12405215

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Standard

Height

near SLC5A12 · rs12363428

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Showing 20 of 9402 · page 24 of 471

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.