rs9372625
▶GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (5)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
gastroesophageal reflux disease
Ong JS et al. “Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis.” Gut 71(6):1053-1061 (2022)
Allele G
OR —
β 0.038
p 3.0e-14
N 602,604
Large GWAS
European
cognitive domain measurement
Schoeler T et al. “Combining cross-sectional and longitudinal genomic approaches to identify determinants of cognitive and physical decline.” Nature Communications 16(1):4524 (2025)
Allele G
OR 0.02
p 2.0e-12
N 158,996
Large GWAS
European
digestive system disease, abdominal abscess
Tängdén T et al. “A genome-wide association study in a large community-based cohort identifies multiple loci associated with susceptibility to bacterial and viral infections.” Scientific Reports 12(1):2582 (2022)
Allele A
OR 0.95
p 2.0e-9
N 337,484
Large GWAS
European
sexual activity behaviour attribute
Zietsch BP et al. “Genomic evidence consistent with antagonistic pleiotropy may help explain the evolutionary maintenance of same-sex sexual behaviour in humans.” Nature Human Behaviour 5(9):1251-1258 (2021)
Allele G
OR 0.11
p 2.0e-8
N 358,426
Large GWAS
European
Karlsson Linnér R et al. “Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.” Nature Genetics 51(2):245-257 (2019)
Allele G
OR 0.01
p 4.0e-8
N 370,711
Large GWAS
European
risk-taking behaviour
Karlsson Linnér R et al. “Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.” Nature Genetics 51(2):245-257 (2019)
Allele A
OR 0.01
p 3.0e-8
N 404,291
Large GWAS
European
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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