Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,360 positions on this site are linked to Height, out of 107,852 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)

GRB10 · rs10235705

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Standard

Height

ADCY1 · rs10225980

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Standard

Height

near SBF1P2 · rs1009592

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Standard

Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

LINC02227 · rs10044492

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Standard

Height

LINC01725 · rs9787364

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Standard

Height

ANO1 · rs9630219

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Standard

Height (baseline)

near LNX2 · rs9581878

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Standard

Height

BMP6 · rs9505276

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Standard

Height (baseline)

near HMGN1P19 · rs856586

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Standard

Height

ETS2-AS1 · rs8131592

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Standard

Height (baseline)

LINC01574 · rs812817

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Standard

Height

WFDC1 · rs8051764

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Standard

Height

GALNT1 · rs79641095

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Standard

Height

near Y_RNA · rs7902725

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Standard

Height (standard GWA)

near RPS26 · rs78865465

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Standard

Height (standard GWA)

LINC01505 · rs7861738

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Standard

Height (standard GWA)

near FIGN · rs77559470

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Standard

Height

PRKN · rs7742310

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Standard

Height (baseline)

ZNF438 · rs75511418

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Standard

Height (baseline)

near WNT7B · rs75427302

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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.