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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,639 positions on this site are linked to Height, out of 2,511,526 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

SPRY4-AS1 · rs253438

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Standard

Height

PHF20 · rs2425163

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Standard

Height

LMO7 · rs9318373

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Standard

Height

AKT3 · rs14403

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Standard

Height

RABGAP1 · rs803733

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Standard

Height

SMG6-AS1 · rs16951881

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Standard

Standing height (UKB data field 50)

BMP6 · rs553291419

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Standard

Height

STPG4 · rs10460536

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Standard

Height

DRAIC · rs88505

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Standard

Height

SBNO2 · rs740495

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Standard

Height

LTBP1 · rs218197

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Standard

Height

H1-10-AS1 · rs6763292

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height (mean, inv-normal transformed)

IGF2BP3 · rs11769151

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Height

COL12A1 · rs240724

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Height

PSMD13 · rs2272566

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Height (baseline)

FAF1 · rs113836734

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Standard

Height

TRIM6-TRIM34 · rs3751006

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height (minimum, inv-normal transformed)

near TRIP11 · rs67015182

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Standard

Height

EGR3-AS1 · rs2313167

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Height

ANKRD52 · rs72648137

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Showing 20 of 11639 · page 1 of 582

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.