Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,794 positions on this site are linked to Height, out of 112,691 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)

CDK6-AS1 · rs77489095

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Standard

Height (baseline)

TENT5A · rs75451347

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Standard

Height (baseline)

near NMB · rs531061098

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Standard

Height (baseline)

WNT5A · rs815540

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Standard

Height (baseline)

RALY · rs75912699

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Standard

Height (baseline)

CHRNB1 · rs530436279

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Standard

Height (baseline)

ZSCAN2-AS1 · rs3762168

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Standard

Height

PRRX1 · rs2213751

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Standard

Height (baseline)

near U6 · rs140282896

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Standard

Height (standard GWA)

ZNF628 · rs73057171

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Standard

Height

CMIP · rs6564905

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Standard

Height

near MRPS11P1 · rs4814999

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Standard

Standing height (UKB data field 50)

near LINC02571 · rs113300871

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Standard

Height (baseline)

LIN28B · rs62419605

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Standard

Height (baseline)

MFGE8 · rs28384224

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Standard

Height

ADAR · rs2335230

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Standard

Height

CRHR1 · rs17689882

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Standard

Height

NCOA2 · rs16936922

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Standard

Height

GLI3 · rs11983409

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Standard

Height

near CBX7 · rs738469

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Showing 20 of 9794 · page 429 of 490

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.