Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
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
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
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
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151