Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs779027563 0.677 0.360 17 42687838 missense variant G/C snv 4.0E-06 7.0E-06 58
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 46
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1555038111 0.701 0.480 11 118478153 stop gained T/G snv 37
rs180177035 0.752 0.280 7 140801502 missense variant T/C snv 35
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 34
rs1557781252 0.742 0.320 1 153816414 stop gained G/A snv 33
rs1034395178 0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs121918455 0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs66527965 0.763 0.240 17 50193038 missense variant C/A;T snv 29
rs180177135 0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 27
rs77078070 0.742 0.280 7 23165737 stop gained C/T snv 1.2E-05 1.4E-05 26
rs398124401 0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 25
rs121918487 0.716 0.440 10 121517378 missense variant C/A;G;T snv 24
rs121918494 0.790 0.160 10 121517363 missense variant G/C snv 24
rs142239530 0.790 0.320 11 4091328 missense variant C/G;T snv 4.4E-05 24
rs1564919048 0.732 0.280 10 121520106 missense variant C/A snv 23
rs121918467 0.807 0.280 12 112486482 missense variant C/A;T snv 8.0E-06; 1.2E-05 23
rs886043994 0.776 0.400 20 32433355 frameshift variant GT/- delins 21