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: rs10168266
rs10168266
0.801 0.250 2 191071078 intron variant C/T snp 0.19
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Digestive System Diseases 0.700 1 2017 2017
dbSNP: rs3024921
rs3024921
0.878 0.071 2 191078546 intron variant A/T snp 4.2E-02
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Digestive System Diseases 0.700 1 2012 2012
dbSNP: rs7574865
rs7574865
0.618 0.571 2 191099907 intron variant T/G snp 0.79
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Digestive System Diseases 0.700 1 2012 2012