Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1081105 1.000 0.080 19 44909698 non coding transcript exon variant A/C snv 3.0E-02 1
rs1167428194 1.000 0.080 19 44908634 missense variant A/C snv 1
rs28931579 19 44909236 missense variant A/C snv 9.5E-05 6.3E-05 1
rs121918394 0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs115299243 19 44907291 non coding transcript exon variant A/G snv 7.1E-03 1
rs1275147925 1.000 0.080 19 44906613 missense variant A/G snv 7.0E-06 1
rs28931576 19 44907894 missense variant A/G snv 1.2E-05 1.4E-05 1
rs397514253 1.000 0.080 19 44908531 splice acceptor variant A/G snv 1
rs449647 0.925 0.120 19 44905307 upstream gene variant A/T snv 0.21 2
rs1424027593 1.000 0.080 19 44908639 missense variant C/A snv 1
rs981058595 1.000 0.080 19 44908847 missense variant C/A snv 1
rs11542029 1.000 0.080 19 44907864 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.2E-05 1
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs121918393 0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs11542037 1.000 0.080 19 44908657 missense variant C/A;T snv 5.2E-06 1
rs121918395 19 44909032 missense variant C/A;T snv 6.9E-06; 4.2E-05 1
rs868094551 1.000 0.080 19 44908768 missense variant C/A;T snv 1
rs267606661 0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs573658040 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs440446 0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs387906567 0.882 0.200 19 44908774 missense variant C/G;T snv 6.3E-06 4
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs764929617 0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs769455 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs121918399 0.925 0.120 19 44907843 missense variant C/T snv 8.0E-06 2