Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,487 positions on this site are linked to Height, out of 2,509,560 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

LINC01505 · rs10115173

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Standard

Height (baseline)

near LINC00917 · rs9923266

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Standard

Height

CAST · rs9918149

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Standard

Height

PPARD · rs9658118

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Standard

Height

near RNU6-669P · rs9409567

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Standard

Height

EFCAB6-DT · rs8138497

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Standard

Height

LINC02464 · rs7968353

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Standard

Height (baseline)

GPR149 · rs789298

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Standard

Height (baseline)

NCOA1 · rs78500502

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Standard

Height (baseline)

near Y_RNA · rs78331472

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Standard

Height

near INHBA-AS1 · rs7805201

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Standard

Height (baseline)

near GUSBP5 · rs77887721

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Standard

Height (standard GWA)

near RPSAP20 · rs778412

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Standard

Height (baseline)

TFEB · rs77542887

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Standard

Height (baseline)

GALNS · rs77318452

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Standard

Height (baseline)

near HLA-DRB9 · rs76252686

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Standard

Height

near SMAD6 · rs76132480

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Standard

Height

near ID2-AS1 · rs7606528

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Standard

Height (baseline)

near POM121L2 · rs76054911

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Standard

Height (baseline)

near RPL21P18 · rs75566446

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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.