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 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,432 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 (baseline)

LYN · rs62515386

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Standard

Height

GALR1 · rs58980065

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Standard

Height

RIC3 · rs4758295

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Standard

Height (baseline)

near PNPT1 · rs1579494

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Standard

Height (baseline)

near RPS10P13 · rs572697180

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Standard

Height (baseline)

near RETREG2 · rs74187143

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Standard

Height

CFAP299 · rs6816536

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Standard

Height

EIF4G3 · rs17449243

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Standard

Height

GLIS2 · rs9938257

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Standard

Height

GNGT2 · rs4793612

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Standard

height (mean, inv-normal transformed)

near AK4P2 · rs4635901

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Standard

Standing height (UKB data field 50)

FBN1 · rs8026752

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Standard

Height (baseline)

TRPC4AP · rs76223987

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Standard

Height

near GALNT1 · rs7241221

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Standard

Height (baseline)

IRAIN · rs28869768

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Standard

Height (baseline)

near CD83P1 · rs72845030

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Standard

Height

PDGFD · rs10791660

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Standard

Height

MIR29B2CHG · rs4844620

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Standard

Height

near ERP29 · rs4767293

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Standard

Height (baseline)

ZBTB38 · rs34544234

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Showing 20 of 11114 · page 198 of 556

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.