Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,995 positions on this site are linked to Height, out of 115,002 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

GIGYF2 · rs894857163

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Standard

Height (baseline)

near CRADD · rs80307446

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Standard

Height (baseline)

FLYWCH2 · rs79424176

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Standard

Height (baseline)

KLHL29 · rs78926083

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Standard

Height (baseline)

near SMG1P5 · rs77016006

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Standard

Height (baseline)

PNPLA1 · rs76228061

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Standard

Height

PTBP2 · rs7513314

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Standard

Height (baseline)

THRB-AS2 · rs74956157

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Standard

Height

FHAD1 · rs736185

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Standard

Height (baseline)

IGF1 · rs73180982

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Standard

Height (baseline)

ACAN · rs72765681

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Standard

Height

LINC01081 · rs7201739

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Standard

Height (baseline)

CCND2-AS1 · rs71458092

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Standard

Height (baseline)

LIN28B · rs6902142

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Standard

Height (baseline)

SLC7A15P · rs6531236

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Standard

Height

TANC2 · rs6504154

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Standard

Height (baseline)

near STK31 · rs61390035

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Standard

Height

EPB41L1 · rs6060844

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Standard

Height (baseline)

WASHC3 · rs56256745

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Standard

Height (baseline)

ME1 · rs45524131

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Showing 20 of 9995 · page 86 of 500

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.