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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs2857766
MOG
0.882 0.120 6 29666226 missense variant G/C snv 0.22 0.19 4