Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs118192116 0.784 0.107 19 38451850 missense variant C/G,T snp 4.0E-06 3.2E-05 7
rs118192153 0.784 0.107 19 38585013 missense variant C/G,T snp 1.2E-05; 4.0E-06 3.2E-05 7
rs118192161 0.784 0.107 19 38444211 missense variant snp 7
rs118192162 0.784 0.107 19 38455359 missense variant A/C,G snp 7
rs118192163 0.784 0.107 19 38494565 missense variant G/A,C snp 7
rs118192168 0.769 0.143 19 38580403 missense variant G/A snp 1.6E-05 3.2E-05 7
rs118192172 0.784 0.107 19 38457545 missense variant C/T snp 8.7E-05 2.6E-04 7
rs118192176 0.769 0.143 19 38494579 missense variant G/A snp 7
rs118192178 0.784 0.107 19 38500898 stop gained C/G,T snp 7
rs193922748 0.784 0.107 19 38440829 stop gained C/T snp 4.1E-06 7
rs28933396 0.784 0.107 19 38499997 missense variant G/A,T snp 7
rs63749869 0.784 0.107 19 38580440 missense variant G/A snp 7
rs118192167 0.801 0.107 19 38580004 missense variant A/G snp 5
rs118192170 0.801 0.107 19 38584989 missense variant T/C snp 5
rs375915752 0.923 0.036 19 38529048 missense variant C/G,T snp 4.0E-06; 4.0E-06 2
rs763259167 0.923 0.036 19 38525377 missense variant G/T snp 4.0E-06 2
rs111272095 0.923 0.036 19 38466347 missense variant C/T snp 2.9E-05 2
rs111364296 0.923 0.036 19 38499817 missense variant G/A snp 3.0E-05 6.4E-05 2
rs111565359 0.923 0.036 19 38535197 missense variant G/A snp 2
rs111657878 0.923 0.036 19 38585947 missense variant T/C snp 2
rs111888148 0.923 0.036 19 38455463 stop gained G/A,T snp 5.6E-05 2
rs112151058 0.923 0.036 19 38517541 missense variant G/A,C snp 2
rs112196644 0.923 0.036 19 38504869 missense variant A/G snp 2
rs112563513 0.923 0.036 19 38499223 missense variant G/A snp 2
rs112596687 0.923 0.036 19 38446517 missense variant T/A,C,G snp 4.0E-06; 4.0E-06 2