Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
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
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193