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
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61