rs1782810
This variant is located in the MIR137HG 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.
autism spectrum disorder, schizophrenia
“Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.” Molecular Autism 8:21 (2017)
Allele A
OR 1.12
p 1.0e-19
N 17,968
Meta-analysisLarge GWAS
European
About MIR137HG
Predicted to be involved in miRNA-mediated post-transcriptional gene silencing. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Jul 2025]
View all MIR137HG variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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