rs57749775, KRT8

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Cirrhosis, Cryptogenic
CUI: C0267809
Disease: Cirrhosis, Cryptogenic
5 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 0.700 0
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 0.010 1.000 1 2003 2003
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 0.010 1 2004 2004
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 0.010 1.000 1 2003 2003
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 0.010 1.000 1 2006 2006
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 0.010 1.000 1 2006 2006