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: rs72653170
rs72653170
10 0.752 0.240 17 50188908 missense variant G/A snv 8.0E-06 0.700 0
dbSNP: rs66527965
rs66527965
31 0.763 0.240 17 50193038 missense variant C/A;T snv 0.700 0
dbSNP: rs66612022
rs66612022
9 0.763 0.240 7 94409768 missense variant G/A;T snv 0.700 0
dbSNP: rs72659319
rs72659319
9 0.763 0.240 7 94426459 missense variant G/A;C snv 0.700 0
dbSNP: rs67543427
rs67543427
8 0.776 0.240 7 94410457 missense variant G/A;T snv 0.700 0
dbSNP: rs72645357
rs72645357
8 0.776 0.240 17 50196163 missense variant C/T snv 0.700 0
dbSNP: rs1555574303
rs1555574303
7 0.790 0.240 17 50196172 missense variant C/G snv 0.700 0
dbSNP: rs66490707
rs66490707
7 0.790 0.240 17 50195231 splice donor variant C/G;T snv 0.700 0
dbSNP: rs66555264
rs66555264
7 0.790 0.240 17 50192993 splice donor variant C/A;T snv 0.700 0
dbSNP: rs67879854
rs67879854
7 0.790 0.240 17 50190578 missense variant C/A;T snv 0.700 0
dbSNP: rs72648326
rs72648326
7 0.790 0.240 17 50195288 stop gained G/A snv 0.700 0
dbSNP: rs72651642
rs72651642
7 0.790 0.240 17 50191826 stop gained G/A snv 7.0E-06 0.700 0
dbSNP: rs72656332
rs72656332
3 0.882 0.120 17 50186895 missense variant C/T snv 0.700 0
dbSNP: rs768171831
rs768171831
3 0.882 0.120 7 94426011 missense variant C/T snv 1.2E-04; 4.0E-06 5.6E-05 0.700 0
dbSNP: rs1057516036
rs1057516036
4 0.925 0.160 7 94423065 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs121912902
rs121912902
2 0.925 0.120 7 94424363 missense variant G/A snv 0.700 0
dbSNP: rs121912906
rs121912906
2 0.925 0.120 7 94412593 missense variant G/T snv 0.700 0
dbSNP: rs121912910
rs121912910
2 0.925 0.120 7 94413083 missense variant G/A snv 0.700 0
dbSNP: rs66929517
rs66929517
2 0.925 0.120 17 50190334 missense variant C/A;G snv 0.700 0
dbSNP: rs72645333
rs72645333
2 0.925 0.120 17 50196651 missense variant C/T snv 0.700 0
dbSNP: rs72648333
rs72648333
2 0.925 0.120 17 50195099 missense variant C/A snv 0.700 0
dbSNP: rs72648356
rs72648356
2 0.925 0.120 17 50194365 missense variant C/T snv 0.700 0
dbSNP: rs72648363
rs72648363
2 0.925 0.120 17 50194005 missense variant C/G snv 0.700 0
dbSNP: rs72651646
rs72651646
2 0.925 0.120 17 50191462 missense variant C/T snv 0.700 0
dbSNP: rs72651651
rs72651651
2 0.925 0.120 17 50191408 missense variant C/G;T snv 0.700 0