Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs267606870 0.763 0.280 15 90088703 missense variant G/A;C snv 6
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs80338963 0.776 0.280 18 51065548 missense variant C/A;G;T snv 11
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 9
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25