Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs769449 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
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
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
rs121918393 0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs769446 0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 6
rs121918394 0.882 0.080 19 44908786 missense variant A/C;G snv 6.5E-06 5
rs140808909 0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs267606664 0.851 0.120 19 44908730 missense variant G/A;C snv 1.6E-04; 6.3E-06 5
rs769450 0.925 0.120 19 44907187 non coding transcript exon variant G/A snv 0.39 5
rs1233347077 0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs199768005 0.882 0.160 19 44909057 missense variant T/A snv 4.5E-04 4.9E-04 4
rs387906567 0.882 0.200 19 44908774 missense variant C/G;T snv 6.3E-06 4
rs752600356 0.851 0.280 19 44908681 missense variant G/A;C snv 2.3E-05 1.4E-05 4
rs761592007 0.882 0.160 19 44909013 missense variant G/A snv 1.5E-05 4
rs121918397 0.882 0.200 19 44908784 missense variant G/A;C snv 6.5E-06 3
rs190853081 0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3
rs267606663 0.925 0.080 19 44909021 missense variant G/A;C snv 7.3E-06 3
rs748703149 0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3