Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs2745557 0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214