rs7141420

This variant is located in the NRXN3 gene.

GWAS Catalog Trait Associations (8)

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

body mass index

Koskeridis F et al. Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Nature Communications 13(1):6939 (2022)
Allele T
OR 0.02
p 5.0e-38
N 694,649
Large GWAS
European
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.02
p 4.0e-19
N 523,818
Large GWAS
multi-ancestry
Allele T
OR 0.02
p 2.0e-37
N 434,794
Meta-analysisLarge GWAS
European
Allele T
OR 0.02
p 1.0e-25
N 394,642
Large GWAS
European
Allele T
OR
β 0.027
p 1.0e-24
N 309,889
Large GWAS
European
Allele T
OR 0.03
p 1.0e-11
N 238,944
Large GWAS
multi-ancestry
Allele T
OR 0.02
p 7.0e-15
N 158,284
Large GWAS
multi-ancestry
Allele T
OR 0.02
p 4.0e-11
N 153,041
Meta-analysisLarge GWAS
multi-ancestry
Allele T
OR 0.03
p 4.0e-10
N 123,097
Meta-analysisLarge GWAS
multi-ancestry

body weight

Allele T
OR 0.02
p 4.0e-33
N 394,642
Large GWAS
European

base metabolic rate measurement

Allele T
OR 0.01
p 1.0e-26
N 394,642
Large GWAS
European

whole body water mass

Allele T
OR 0.01
p 2.0e-22
N 394,642
Large GWAS
European

obesity

Allele T
OR 1.08
p 1.0e-17
N 204,498
Meta-analysisLarge GWAS
European

lean body mass

Harris BHL et al. New role of fat-free mass in cancer risk linked with genetic predisposition. Scientific Reports 14(1):7270 (2024)
Allele T
OR 0.01
p 4.0e-15
N 337,739
Large GWAS
European

physical activity measurement, body mass index

Allele T
OR 0.02
p 2.0e-12
N 161,368
Meta-analysisLarge GWAS
multi-ancestry

smoking behavior, body mass index

Allele T
OR 0.02
p 5.0e-12
N 196,760
Meta-analysisLarge GWAS
multi-ancestry

About NRXN3

This gene encodes a member of a family of proteins that function in the nervous system as receptors and cell adhesion molecules. Extensive alternative splicing and the use of alternative promoters results in multiple transcript variants and protein isoforms for this gene, but the full-length nature of many of these variants has not been determined. Transcripts that initiate from an upstream promoter encode alpha isoforms, which contain epidermal growth factor-like (EGF-like) sequences and laminin G domains. Transcripts initiating from the downstream promoter encode beta isoforms, which lack EGF-like sequences. Genetic variation at this locus has been associated with a range of behavioral phenotypes, including alcohol dependence and autism spectrum disorder. [provided by RefSeq, Dec 2012]

View all NRXN3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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