Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057141
rs1057141
1 1.000 0.080 6 32850997 missense variant T/C snv 0.20 0.20 0.010 1.000 1 2016 2016
dbSNP: rs1135216
rs1135216
6 0.807 0.200 6 32847198 missense variant T/C snv 0.17 0.18 0.010 1.000 1 2016 2016