rs17036101
▶GWAS Catalog Trait Associations (9)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (9)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
serum albumin amount
serum alanine aminotransferase amount
aspartate aminotransferase to alanine aminotransferase ratio
blood protein amount
sex hormone-binding globulin measurement
serum gamma-glutamyl transferase measurement
triglyceride measurement
calcium measurement
adipose amount
▶Research that mentions this SNP (2)
▶Correcting “winner's curse” in odds ratios from genomewide association findings for major complex human diseasesMethodsHua Zhong et al.(2010)· Genetic Epidemiology
This paper applies a bias correction method for odds ratio estimates from GWAS discovery data, demonstrating that the 'winner's curse' affects initial effect size estimates. The authors applied conditional maximum likelihood estimation to correct bias in GWAS findings from multiple complex diseases (breast cancer, colorectal cancer, lung cancer, prostate cancer, type I and II diabetes) and show that bias-adjusted odds ratios are substantially more consistent with subsequent replication studies, with selection-adjusted confidence intervals providing better uncertainty quantification than uncorrected estimates.
▶Replication study for the association of new meta-analysis-derived risk loci with susceptibility to type 2 diabetes in 6,244 Japanese individualsAssociationN=6,244Omori S. et al.(2009)· Diabetologia
Replication study of 7 meta-analysis-derived type 2 diabetes susceptibility SNPs in 6,244 Japanese individuals across 3 independent populations. Only rs864745 in JAZF1 showed nominal association (OR 1.148, 95% CI 1.034-1.275, p=0.0098) but not after Bonferroni correction; other loci did not reach statistical significance, suggesting these European-identified variants have minor or absent effects in Japanese populations.
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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