Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1057519862 0.851 0.160 17 39723405 missense variant G/A snv 5
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519956 0.827 0.200 2 218583025 missense variant T/C snv 5
rs1057519957 0.827 0.200 2 218583026 missense variant C/G snv 5
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913228 0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913407 0.763 0.240 3 41224645 missense variant T/C;G snv 12