Variants linked to Height

Continuously updated · newest added Oct 24, 2026

10,072 positions on this site are linked to Height, out of 115,842 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

CNTN3 · rs6549596

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Standard

Height

LETR1 · rs6496101

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Standard

Height (baseline)

NPR2 · rs61758515

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Standard

Height (baseline)

near FLNB · rs58008947

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Standard

Height (baseline)

near GSTM2P1 · rs55710344

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Standard

Height (baseline)

MEIKIN · rs541065095

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Standard

Height

near ANAPC16 · rs4595469

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Standard

Height (baseline)

POLR2A · rs41556717

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Standard

Height (baseline)

near MTF2 · rs34948837

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Standard

Height (baseline)

PSMA1 · rs2575863

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Standard

Height

FBXO24 · rs2272575

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Standard

Height

near TRIB2 · rs2098824

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Standard

Height (baseline)

near LINC00243 · rs201764091

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Standard

Height (baseline)

RFT1 · rs189930739

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Standard

Height

LINC00973 · rs1879378

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Standard

Height (baseline)

LINC00924 · rs184332341

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Standard

Height

near MTCO2P25 · rs17751099

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Standard

Height

POLR1D · rs17072022

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Standard

Height (baseline)

RSRC1 · rs16828986

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Standard

Height

LINC01121 · rs1559475

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Showing 20 of 10072 · page 93 of 504

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.