Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs63751287 0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs1057518919 0.851 0.120 14 73171023 missense variant T/G snv 5
rs544706237 0.851 0.120 2 79121649 missense variant A/G;T snv 8.0E-06; 5.2E-05 5
rs747105516 0.851 0.120 7 56015139 missense variant T/C snv 4.0E-06 5
rs63751011 0.925 0.120 17 46010418 intron variant C/T snv 4