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

11,323 positions on this site are linked to Height, out of 2,508,068 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

ADAM28 · rs1013209

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Standard

Height

LYPLAL1 · rs11118346

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Standard

Height

PCCB · rs9844666

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Standard

Height

PEX2 · rs6473015

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Standard

Height

HLA locus · rs6457620

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Standard

Height

BOD1 · rs889014

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Standard

Height

OR2J3 · rs3129109

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Standard

Height

C3orf47 · rs6439167

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Standard

Height

IGF2BP3 · rs12534093

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Height

H6PD · rs6662509

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Standard

Height

BMP6 · rs1885486

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Height

FER · rs13177718

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Height

MYO9A · rs12902421

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Height

STAT2 · rs2066807

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Height

SENP6 · rs9360921

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Height

C2orf52 · rs6750795

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Height

PPARD/FANCE · rs6457821

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Height

IPPK · rs9969804

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Height

DNAJC27 · rs4665736

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Standard

Height

NUCB2 · rs1330

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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.