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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 12