Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205