Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057520036 0.925 0.080 5 177093180 missense variant A/G snv 1
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 9
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
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
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 9
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 10
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 11
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs121913285 3 179218286 missense variant C/G snv 1
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14