Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129878 0.807 0.360 6 32440958 intron variant A/C snv 0.30 6
rs9268644 0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1805010 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 12
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1059288 0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 3
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2844484 0.807 0.320 6 31568447 upstream gene variant A/G snv 0.64 6
rs3129943 0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
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
rs4505848 0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs72661131 0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15