Gene Knowledge Graph
UTC

Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,879 positions on this site are linked to Height, out of 113,615 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Standard

height (mean, inv-normal transformed)

ZNF878 · rs67102109

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Height (baseline)

near LCORL · rs6449356

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Height

MICAL3 · rs415651

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Height (baseline)

near SOCS2 · rs117743355

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Height (baseline)

CHEK2 · rs7287609

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Height

RTN4RL1 · rs4239060

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Height

KCNQ1 · rs41517049

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Standing height (UKB data field 50)

FHIP1A · rs2709814

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Height (baseline)

L3MBTL3 · rs117495878

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Height (baseline)

SFRP4 · rs10435160

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Height (baseline)

near RNU6-650P · rs73725441

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height (minimum, inv-normal transformed)

ZNF433-AS1 · rs73000424

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Height

near LINC00583 · rs717605

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Height (baseline)

BCKDHB · rs527628111

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Height (baseline)

near NAP1L1P1 · rs511987

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Standing height (UKB data field 50)

H2AJ · rs3789999

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Height (baseline)

RTF1 · rs316612

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Standing height (UKB data field 50)

CFL1P1 · rs17101804

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Height (baseline)

EPB41L2 · rs11967564

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Height

IGFBP4 · rs598892

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Showing 20 of 9879 · page 424 of 494

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.