Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,304 positions on this site are linked to Height, out of 107,180 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 (baseline)

TNRC18 · rs80186772

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Standard

Height

near RNY1P8 · rs8002827

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Standard

Height (baseline)

near BNC1 · rs79722445

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Standard

Height

LRRC4C · rs7929217

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Standard

Height

ATRNL1 · rs7911480

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Standard

Height

GRAMD2B · rs7704203

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Standard

Height (baseline)

KPNA7 · rs76888365

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Standard

Height (baseline)

XXYLT1 · rs73206626

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Standard

Height (baseline)

XPO4 · rs73167443

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Standard

Height (baseline)

ADGRD1 · rs7312364

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Standard

Height (baseline)

near RGS9 · rs72853511

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Standard

Height (baseline)

ADCY3 · rs72792187

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Standard

Height (baseline)

near IARS1 · rs72748400

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Standard

Height (baseline)

near RNU6-506P · rs72724774

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Standard

Height

near GDPD5 · rs7128888

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Standard

Height

near SLC45A4 · rs6992945

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Standard

Height

near MRPL42P4 · rs6955374

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Standard

Height

GLIS1 · rs67752113

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Standard

Height

LALTOP · rs6721842

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Standard

Height (baseline)

near LINC01819 · rs6719452

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Showing 20 of 9304 · page 11 of 466

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.