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

SPTBN1 · rs966003

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Standard

Height (baseline)

near C11orf86 · rs4930188

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Standard

Height

near INSM2 · rs1958258

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Standard

Height (standard GWA)

SPON1 · rs74404771

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Standard

Height

near LINC02527 · rs58157605

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Standard

Height (baseline)

PNKD · rs56411817

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Standard

Height

LHFPL3-AS1 · rs2470961

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Standard

Height (baseline)

near SFTPA2 · rs17884590

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Standard

Height

NFIA · rs6693597

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Standard

Height

COPZ1 · rs574708537

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Standard

Height

near SERTAD4 · rs55645018

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Standard

Height

near ABCC10 · rs4714680

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Standard

Height (baseline)

GYPA · rs372519407

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Standard

Height (baseline)

ANO1 · rs34094842

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Standard

Height (baseline)

PCGF6 · rs117502120

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Standard

Height

CENPT · rs11558533

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Standard

Height (baseline)

near SSH3 · rs111908242

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Standard

Height

MAPK1 · rs9610500

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Standard

Height (baseline)

LINC02136 · rs80223220

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Standard

Height (baseline)

SCAMP2 · rs62006636

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Showing 20 of 10072 · page 411 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.