Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs2241715 0.851 0.120 19 41350981 5 prime UTR variant A/C snv 0.68 4
rs2244444 0.882 0.080 1 17520426 intergenic variant C/T snv 0.55 3
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs2299939 0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs230496 0.882 0.080 4 102567334 intron variant G/A snv 0.59 3
rs230525 0.882 0.080 4 102537720 non coding transcript exon variant G/A snv 0.69 4
rs230530 0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193