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 12, 2026

11,888 positions on this site are linked to Height, out of 2,516,241 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 RN7SKP15 · rs7304170

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Standard

Height

MICA-AS1 · rs7775759

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Height

ATXN10 · rs136029

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Height

TRA2B · rs2300921

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Height

near SDC1 · rs6749689

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Height

SLC12A2 · rs790156

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Height

CRADD · rs9788269

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Height

ZNF831 · rs882384

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Height

ZFP1 · rs9939124

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Height

IGF2BP1 · rs2969

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Height

RSRC1 · rs827154

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Height

RPS10-NUDT3 · rs7775497

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Height

near ECM1P2 · rs11726001

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Height

near H6PD · rs9434723

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Height

near LINC01713 · rs6140071

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Height

near CDC16 · rs7994556

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Height

TNC · rs1250023

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Height

near PTPRG · rs12108098

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Height

CRIM1 · rs861051

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Height

HHIP-AS1 · rs2035742

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Showing 20 of 11888 · page 72 of 595

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.