Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869312704 0.882 0.160 2 161423752 frameshift variant -/GGCTGCA delins 10
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs145606134 0.882 0.240 X 102937494 missense variant A/G snv 5.4E-03 4.1E-03 5
rs1057519511 1.000 3 9734500 frameshift variant AG/- delins 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs17070145 0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs1555349214 14 36517838 frameshift variant G/- delins 2
rs267606827 0.925 0.120 14 28768203 stop gained G/A snv 3
rs387906726 0.925 0.040 X 15321727 stop gained G/A snv 3
rs1057519522 1.000 10 129877788 stop gained G/A snv 2
rs745638189 1.000 0.040 10 87960997 missense variant G/A snv 4.0E-06 7.0E-06 2
rs949944999 6 27873237 missense variant T/C snv 1