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: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.020 1.000 2 2013 2019
dbSNP: rs10766197
rs10766197
0.807 0.240 11 14900334 upstream gene variant G/A;C snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs12794714
rs12794714
0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs1562902
rs1562902
0.925 0.120 11 14896670 upstream gene variant C/T snv 0.55
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs1993116
rs1993116
0.827 0.200 11 14888688 intron variant A/G snv 0.65
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2013 2013