Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507546 0.790 0.360 12 112489084 missense variant G/A;C;T snv 6
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs121913365 0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs397507484 0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22