[PMID 23543094] Testing for associations between loci and environmental gradients using latent factor mixed models.

rs7665090

Parent Gene: MANBA, NFKB1

Importance: 2
Less common allele: A = 45%
More common allele: G = 55%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Biliary Liver Cirrhosis

The C allele of rs7665090 is reported to be associated with Biliary Liver Cirrhosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Primary biliary cholangitis.