Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 9, 2026

11,375 positions on this site are linked to Height, out of 2,508,576 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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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height (baseline)

ZBTB38 · rs79705096

See detailed info → Standard

Height

near RPL29P17 · rs7761069

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Height (baseline)

PDE12 · rs7641375

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Height

near LINC02409 · rs76107589

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Height

TCN2 · rs740234

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Height

MIRLET7BHG · rs7292297

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Height (baseline)

DDX4 · rs71622199

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Height

near FAM169BP · rs6598516

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Height (standard GWA)

near NCOA4P4 · rs4912716

See detailed info → Standard

Height (baseline)

SYN3 · rs4820085

See detailed info → Standard

Height

CPLANE1-AS1 · rs28429963

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Height (baseline)

near CMPK1P1 · rs2817046

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Height

ADAMTS17 · rs2573625

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Height

CEP350 · rs16855021

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Height (baseline)

PLA2G15 · rs116844179

See detailed info → Standard

Standing height (UKB data field 50)

near NPR3 · rs111984297

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Height

ERLIN1 · rs10509741

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Height

CAMK1D · rs914328

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Height

near PITX1 · rs657223

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Height

near RN7SL547P · rs6133455

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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.