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rs7665590

From SNPedia

Orientationplus
Stabilizedplus
Make rs7665590(C;C)
Make rs7665590(C;T)
Make rs7665590(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position98875633
is asnp
is mentioned by
dbSNPrs7665590
ebirs7665590
HLIrs7665590
Exacrs7665590
Varsomers7665590
Maprs7665590
PheGenIrs7665590
hapmaprs7665590
1000 genomesrs7665590
hgdprs7665590
ensemblrs7665590
gopubmedrs7665590
geneviewrs7665590
scholarrs7665590
googlers7665590
pharmgkbrs7665590
gwascentralrs7665590
openSNPrs7665590
23andMers7665590
23andMe allrs7665590
SNP Nexus

SNPshotrs7665590
SNPdbers7665590
MSV3drs7665590
GWAS Ctlgrs7665590
GMAF0.3976
Max Magnitude
GWAS snp
PMID [PMID 23000144OA-icon.png]
Trait Primary biliary cirrhosis
Title Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population.
Risk Allele G
P-val 1E-7
Odds Ratio 1.35 [1.21-1.52]