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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

10,927 positions on this site are linked to Height, out of 2,505,721 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

Standing height (UKB data field 50)

DCC · rs10502967

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Standard

height (mean, inv-normal transformed)

SH3PXD2A · rs34536993

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Standard

Height

COL24A1 · rs313710

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Standard

Height

LINC02851 · rs1658943

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Standard

height (minimum, inv-normal transformed)

TOX · rs12541161

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Standard

Height

NFIB-AS1 · rs1556032

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Standard

Height

TLCD5 · rs11827818

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Standard

Height (baseline)

near GUSBP5 · rs72731541

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Standard

Standing height (UKB data field 50)

LTBP4 · rs4803348

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Standard

Height (baseline)

BLTP3A · rs144523623

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Standard

Standing height (UKB data field 50)

STAC2 · rs79873275

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Standard

Height

VPS53 · rs410157

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Standard

Standing height (UKB data field 50)

SYNE1 · rs2813536

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Standard

Height (standard GWA)

RPGRIP1 · rs2319817

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Standard

Height (baseline)

near HLA-DRB1 · rs189345292

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Standard

Height

near ARHGAP12 · rs10826995

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Standard

Height

SLC38A9 · rs3846502

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Standard

Standing height (UKB data field 50)

AGRN · rs2001744

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Standard

Height in pregnancy

HELLPAR · rs73386907

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Standard

Height

ADAP2 · rs35840638

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Showing 20 of 10927 · page 532 of 547

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.