rs1563317

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GWAS Catalog Trait Associations (1)

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

rgm domain family member b measurement

Sun BB et al. “Genomic atlas of the human plasma proteome.” Nature 558(7708):73-79 (2018)
Allele G
OR 0.22
p 1.0e-18
N 3,301
Large GWAS
European
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Research that mentions this SNP (1)

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Variants in several genomic regions associated with asperger disorder
AssociationN=860Salyakina D. et al.(2010)· Autism Research

Genome-wide association study in 124 families with Asperger disorder (discovery) and 110 families (validation) identified novel susceptibility loci on 5q21.1 (P = 9.7 × 10⁻⁷, rs4703129) and 15q22.1-q22.2 (P = 7.3 × 10⁻⁶, rs4775101) associated with Asperger disorder. The study confirmed three regions previously linked to Asperger disorder in Finnish families (3p14.2, 3q25-26, 3p23) and identified 26 candidate genes, suggesting that Asperger disorder shares both ASD-related genetic risk factors as well as unique genetic risk factors.

Traits studied:Asperger disorderAutism spectrum disorder
PubMedDOIMetascience Observatory

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

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