Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs1057519943 0.790 0.160 12 132676598 missense variant G/C;T snv 5
rs1057519944 0.882 0.160 12 132676599 missense variant G/A snv 5
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 12
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 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs1057519931 0.827 0.160 3 179199141 missense variant G/C snv 6
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
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
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519738 0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 7