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: rs738409
rs738409
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
Digestive System Diseases 0.100 1.000 45 2009 2019
dbSNP: rs1010023
rs1010023
0.851 0.080 22 43940218 intron variant T/C snv 0.20
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
Digestive System Diseases 0.010 1.000 1 2017 2017