Variants linked to Height

Continuously updated · newest added Oct 23, 2026

9,584 positions on this site are linked to Height, out of 110,133 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

GON4L · rs16837063

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Standard

Height (baseline)

PARK7 · rs161799

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Standard

Height (baseline)

near DNAJC8P1 · rs1543478

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Standard

Height (baseline)

near SPOCD1 · rs1536131

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Standard

Height (baseline)

CPEB1 · rs150684763

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Standard

Height (baseline)

near RNU5A-2P · rs150339689

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Standard

Height (baseline)

LNC-LBCS · rs149529723

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Standard

Height (baseline)

PADI2 · rs148112653

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Standard

Height (baseline)

NCOA1 · rs146555612

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Standard

Height (baseline)

NFX1 · rs146508853

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Standard

Height (baseline)

near ZNF507 · rs145213057

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Standard

Height (baseline)

PCGF5 · rs145206415

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Standard

Height

KC6 · rs142634592

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Standard

Height

HTR7 · rs1418213

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Standard

Height

PTPN4 · rs141607096

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Standard

Height

DELEC1 · rs1411456

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Standard

Height

SGSM1 · rs139663

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Standard

Height (baseline)

PTGES3 · rs139170956

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Standard

Height

ZCCHC10 · rs137876247

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Standard

Height (standard GWA)

near DYSF · rs13384155

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Showing 20 of 9584 · page 39 of 480

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.