Variants linked to Height

Continuously updated · newest added Oct 25, 2026

10,192 positions on this site are linked to Height, out of 117,564 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)

UQCC1 · rs139930072

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Standard

Height

PRICKLE2 · rs1381807

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Standard

Height (baseline)

ZFAT · rs13272130

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Standard

Height (baseline)

near MIR3668 · rs13197876

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Standard

Height

near NKX2-4 · rs13040764

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Standard

Height (baseline)

near BIRC6 · rs13010404

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Standard

Height

near SLFN5 · rs12939024

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Standard

Height (baseline)

NPTN · rs12909389

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Standard

Height

FOXP1 · rs1288829

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Standard

Height

GPC5 · rs12868042

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Standard

Height (standard GWA)

DRAM1 · rs12298720

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Standard

Height

near MTCH2P2 · rs12298192

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Standard

Height

ZBTB16 · rs12275428

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Standard

Height

SLC16A10 · rs1216023

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Standard

Height (baseline)

ZMIZ1 · rs118114823

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Standard

Height (baseline)

near ZNF579 · rs117774922

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Standard

Height (baseline)

near STOML1 · rs117381838

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Standard

Height

near ZFP42 · rs11724392

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Standard

Height (baseline)

near RSPO3 · rs116971072

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Standard

Height (baseline)

SNAP47 · rs115617436

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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.