Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519887 0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs769696078 0.925 0.040 7 55154128 missense variant G/A snv 3
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 17
rs149840192 0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 15
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12