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: rs1057519919
rs1057519919
5 0.851 0.160 2 15942195 missense variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519920
rs1057519920
7 0.790 0.160 2 177234232 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519921
rs1057519921
10 0.763 0.240 2 177234231 missense variant T/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519925
rs1057519925
25 0.683 0.560 3 179210291 missense variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519926
rs1057519926
10 0.776 0.200 3 179210293 missense variant A/T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519927
rs1057519927
19 0.716 0.240 3 179218295 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519929
rs1057519929
10 0.776 0.320 3 179199066 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519931
rs1057519931
6 0.827 0.160 3 179199141 missense variant G/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519932
rs1057519932
22 0.683 0.320 3 179234298 missense variant T/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519933
rs1057519933
11 0.790 0.240 3 179199156 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519934
rs1057519934
11 0.790 0.240 3 179199158 missense variant G/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519935
rs1057519935
11 0.790 0.240 3 179199157 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519936
rs1057519936
11 0.776 0.200 3 179234284 missense variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519937
rs1057519937
11 0.776 0.200 3 179234285 missense variant T/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519938
rs1057519938
10 0.776 0.160 3 179203764 missense variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519939
rs1057519939
10 0.776 0.160 3 179203763 missense variant A/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519940
rs1057519940
13 0.752 0.200 3 179218308 missense variant G/T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519941
rs1057519941
10 0.776 0.240 3 179203761 missense variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519942
rs1057519942
16 0.724 0.320 3 179203760 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519943
rs1057519943
10 0.790 0.160 12 132676598 missense variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519944
rs1057519944
5 0.882 0.160 12 132676599 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519945
rs1057519945
12 0.776 0.200 12 132673703 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
18 0.732 0.280 19 52212729 missense variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
9 0.790 0.160 19 52212730 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519948
rs1057519948
4 0.851 0.120 7 6387262 missense variant C/T snv 0.700 1.000 1 2016 2016