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: rs766264810
rs766264810
1 1.000 0.160 10 95611372 missense variant C/A;T snv 1.2E-05 0.800 0
dbSNP: rs863224945
rs863224945
1 1.000 0.160 10 95637381 missense variant A/G snv 0.800 0
dbSNP: rs864321669
rs864321669
1 1.000 0.160 10 95633040 missense variant C/G snv 0.800 1.000 2 2015 2016
dbSNP: rs864321670
rs864321670
24 0.763 0.320 10 95633012 missense variant C/T snv 0.800 1.000 2 2015 2016