rs57758506, KRT8;KRT18

N. diseases: 3
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 0.882 0.120 12 52949556 missense variant A/T snv 6.3E-04 3.2E-04 0.710 1.000 1 1997 1997
Cirrhosis, Familial
CUI: C1861556
Disease: Cirrhosis, Familial
6 0.882 0.120 12 52949556 missense variant A/T snv 6.3E-04 3.2E-04 0.700 1.000 2 1997 2003
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding)
2 0.882 0.120 12 52949556 missense variant A/T snv 6.3E-04 3.2E-04 0.700 0