Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214