Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1012068
rs1012068
0.827 0.160 22 31869917 intron variant T/G snv 0.37
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.020 1.000 2 2014 2016
dbSNP: rs5998152
rs5998152
0.827 0.160 22 31867176 intron variant T/C snv 0.37
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2014 2014