Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs886039469 0.701 0.560 10 76891709 missense variant T/C snv 35
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs4818 0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs387906686 0.742 0.320 2 165310413 missense variant C/A;T snv 23
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23