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 9, 2026

11,258 positions on this site are linked to Height, out of 2,507,547 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

near PGP · rs27345

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Standard

Height

near EXOSC9 · rs6838153

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Height

near ZC3H11B · rs10746387

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Height

CPZ · rs11723641

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Height

near L3MBTL3 · rs1337775

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Height

CRADD · rs4761530

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Height

NCAPG · rs16895802

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Height

ADCY9 · rs2230742

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Height

EZH1 · rs11657684

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Height

PVT1 · rs1902778

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Height

FILIP1 · rs9360910

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Height

HMGA2 · rs11834900

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Height

near LHX3 · rs11103372

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Height

near PBX4 · rs8113006

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Height

near LINC03007 · rs10238703

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Height

DLEU7 · rs3118917

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Height

INSR · rs12459488

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Height

MIR193BHG · rs30232

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Height

PIEZO1 · rs10775348

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Height

IGF2BP2 · rs6765808

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Showing 20 of 11258 · page 7 of 563

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.