rs376777359
This is a intron variant variant in the SH2D5 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
stomach disease
Verma A et al. “Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.” Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 2.79
p 9.0e-12
N 571,627
Major Consortium StudyLarge GWAS
multi-ancestry
About SH2D5
Predicted to be located in synapse. Predicted to be active in postsynaptic density. [provided by Alliance of Genome Resources, Jul 2025]
View all SH2D5 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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