Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121909219 0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20