Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,982 positions on this site are linked to Height, out of 114,792 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

FOXP1 · rs80190719

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Standard

Height (baseline)

near PRSS38 · rs74140388

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Standard

Standing height (UKB data field 50)

near LINC00681 · rs4510865

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Standard

Height (baseline)

SMAD7 · rs3764482

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Standard

Height (baseline)

near ZNF322 · rs371116791

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Standard

Height (baseline)

PIEZO1 · rs2926774

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Standard

Height

ACAN · rs146576224

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Standard

Height (baseline)

DNMT3A · rs141473447

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Standard

Standing height (UKB data field 50)

IGF1R · rs12907693

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Standard

Standing height (UKB data field 50)

HIVEP2 · rs12154082

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Standard

Height (baseline)

GNPTAB · rs117466029

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Standard

Height (baseline)

SLC38A4 · rs7963364

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Standard

Height (baseline)

NMRAL2P · rs57350994

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Standard

Height (standard GWA)

NOXO1 · rs4305019

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Standard

Standing height (UKB data field 50)

NFIC · rs3764589

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Standard

Height (baseline)

IGF1R · rs2684812

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Standard

Height (baseline)

near PREX1 · rs151072670

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Standard

Standing height (UKB data field 50)

near RNA5SP200 · rs13186631

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Standard

Standing height (UKB data field 50)

near LCORL · rs113261436

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Standard

Height (baseline)

NAV3 · rs11104829

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Showing 20 of 9982 · page 416 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.