Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 15
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 10
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 16
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71