Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,323 positions on this site are linked to Height, out of 2,508,068 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

CRISPLD2 · rs7204018

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Standard

Height

DGKH · rs4142110

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Standard

Height

CAMK1D · rs3802560

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Standard

Height

LINC03007 · rs17368788

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Standard

Height

FAF2 · rs11027

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Standard

Height

SMCHD1 · rs1561819

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Standard

Height

LINC02160 · rs11744391

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Standard

Height

near THBS2-AS1 · rs12665286

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Standard

Height

MIRLET7BHG · rs3744749

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Standard

Height

near ANKS3 · rs841217

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Standard

Height

near RN7SL7P · rs2188177

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Standard

Height (baseline)

CCDC91 · rs11049376

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Standard

height (mean, inv-normal transformed)

ADAMTSL3 · rs11855967

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Standard

Height

RMND1 · rs7771156

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Standard

Height

PLPPR1 · rs4998243

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Standard

Height

near TRMT44 · rs1949733

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Standard

height (minimum, inv-normal transformed)

near PRKG2 · rs3098970

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Standard

Height

CMIP · rs2966116

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Standard

Height

near RNY4P18 · rs1978304

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Standard

Height

ZBTB4 · rs3853894

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Showing 20 of 11323 · page 6 of 567

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.