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: rs1085308044
rs1085308044
5 0.882 0.120 10 87864504 missense variant A/C snv 0.700 0
dbSNP: rs1085308045
rs1085308045
8 0.807 0.160 10 87933128 missense variant C/G;T snv 0.700 0
dbSNP: rs1085308046
rs1085308046
9 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
dbSNP: rs1085308048
rs1085308048
6 0.851 0.320 10 87933175 stop gained T/G snv 0.700 0
dbSNP: rs1085308051
rs1085308051
6 0.882 0.200 10 87933229 missense variant A/G snv 4.0E-06 0.700 0
dbSNP: rs1085308056
rs1085308056
8 0.851 0.160 10 87957850 splice region variant C/G snv 0.700 0
dbSNP: rs121909219
rs121909219
25 0.689 0.400 10 87957915 stop gained C/A;T snv 0.700 0
dbSNP: rs121909231
rs121909231
32 0.667 0.600 10 87961095 stop gained C/A;T snv 0.700 0
dbSNP: rs121913293
rs121913293
18 0.732 0.360 10 87952142 missense variant C/A;T snv 0.700 0
dbSNP: rs587776667
rs587776667
14 0.742 0.280 10 87931090 splice donor variant G/A;C;T snv 0.700 0
dbSNP: rs786202918
rs786202918
6 0.925 0.080 10 87957951 stop gained C/T snv 4.0E-06 0.700 0
dbSNP: rs786204858
rs786204858
11 0.776 0.280 10 87933079 missense variant A/G;T snv 0.700 0