rs12936083

This variant is located in the CHRNE gene.

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GWAS Catalog Trait Associations (1)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

body mass index

Huang J et al. “Genomics and phenomics of body mass index reveals a complex disease network.” Nature Communications 13(1):7973 (2022)

Allele G

OR 0.01

p 4.0e-17

N 1,122,049

Large GWAS

European

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ClinVar annotation

Benign★★★☆

3 submitters1 publication

Congenital myasthenic syndrome; not provided

View on ClinVar →

About CHRNE

Acetylcholine receptors at mature mammalian neuromuscular junctions are pentameric protein complexes composed of four subunits in the ratio of two alpha subunits to one beta, one epsilon, and one delta subunit. The acetylcholine receptor changes subunit composition shortly after birth when the epsilon subunit replaces the gamma subunit seen in embryonic receptors. Mutations in the epsilon subunit are associated with congenital myasthenic syndrome. [provided by RefSeq, Sep 2009]

View all CHRNE variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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