Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2036534 0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 8
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
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
rs1057519729 0.827 0.080 15 66435113 missense variant A/C snv 6
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144