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
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
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23