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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,146 positions on this site are linked to Height, out of 2,506,622 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 (baseline)

LINC01118 · rs112478009

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Standard

Height

near RC3H2 · rs10985794

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Standard

height (mean, inv-normal transformed)

UBN1 · rs8056889

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Standard

Height (baseline)

KCNB1 · rs79333383

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Standard

Height (baseline)

HLA-DRB6 · rs79071881

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Standard

Height (baseline)

ZNF638 · rs7560225

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Standard

Height (baseline)

LHFPL2 · rs72760979

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Standard

Height

near CKB · rs35771849

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Standard

Height

F2RL1 · rs2242993

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Standard

Standing height (UKB data field 50)

CALCR · rs13231861

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Standard

Height (baseline)

COLGALT2 · rs12751980

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Standard

Standing height (UKB data field 50)

JUP · rs12450769

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Standard

Height (baseline)

near RN7SKP208 · rs114896285

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Standard

Height

near RPS16P8 · rs9902474

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Standard

Standing height (UKB data field 50)

COP1-DT · rs76224110

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Standard

Height (baseline)

near GIP · rs72833620

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Standard

Height (baseline)

near ADGRG6 · rs62430524

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Standard

Height (standard GWA)

ENTPD1-AS1 · rs61858612

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Standard

Height (baseline)

near HLA-DRB5 · rs192946774

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Standard

Height (baseline)

LIPH · rs140972670

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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.