Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33