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

11,015 positions on this site are linked to Height, out of 2,505,961 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

H2BC4 · rs16891315

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Standard

Height

ANKFN1 · rs7211753

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Standard

Height

TMEM131L · rs3816086

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Standard

Height

ADAM7-AS1 · rs3736281

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Standard

Height (baseline)

USP4 · rs149972755

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Standard

Height (baseline)

near CABP2 · rs145044531

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Standard

Height

NATD1 · rs12449311

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Standard

Height (baseline)

near ECEL1P3 · rs11682750

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Standard

Height

near LINC01505 · rs9987814

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Standard

Height

RALGAPA2 · rs3748445

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Standard

Height

SMOX · rs6139319

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Standard

Height

near SORL1 · rs528956

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Height

MDFI · rs12661964

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Standard

Height

TRA2A · rs1060974

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Standard

Height

MPP3 · rs4793035

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Standard

Height

PELI2 · rs11626451

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Standard

Height

PIK3R1 · rs706716

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Standard

Height

near RN7SKP199 · rs4132626

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Height

near AK3 · rs396861

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Standard

Height

near SH3YL1 · rs300695

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Showing 20 of 11015 · page 166 of 551

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.