Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27