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
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3734091 0.689 0.280 5 83204915 missense variant G/T snv 2.3E-02 1.4E-02 19
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31