Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19