Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs368087026 0.637 0.520 21 45530890 missense variant G/A snv 33
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19