Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913105 0.724 0.179 4 1806163 missense variant A/C,T snp 16
rs80356624 0.734 0.250 11 17387490 missense variant C/A,T snp 15
rs80356616 0.744 0.321 11 17387917 missense variant C/T snp 12
rs373145711 0.801 0.286 20 32433408 stop gained C/T snp 2.0E-05 6.4E-05 11
rs34767364
NBN
0.734 0.357 8 89971232 missense variant G/A,C snp 2.5E-03 2.0E-03 11
rs80356611 0.801 0.250 11 17387943 missense variant C/G,T snp 4.0E-06 8
rs80356730 0.769 0.107 1 11022418 missense variant A/G snp 8.0E-06 8
rs193929358 0.801 0.250 11 17387091 missense variant C/T snp 6
rs104894885 0.801 0.143 X 119873312 missense variant G/A,C snp 6
rs104894421 0.821 0.214 13 108210436 missense variant C/A,T snp 1.2E-05 3.2E-05 5
rs104894884 0.821 0.107 X 119871933 missense variant G/C snp 5
rs121908869 0.846 0.179 14 80955802 missense variant G/C snp 4.0E-05 5
rs193929353 0.846 0.143 11 17387206 missense variant T/C,G snp 4
rs179363901 0.846 0.107 X 154097661 missense variant G/A snp 4
rs2076101 0.878 0.107 22 39049549 missense variant G/A snp 0.52 0.42 3
rs1057516064 0.878 0.143 MT 9237 missense variant snp 3
rs1057516075 1.000 0.036 MT 15246 missense variant snp 3
rs1135402758 1.000 0.036 9 131199025 intron variant TT/T in-del 3
rs1057518759 0.923 0.071 X 18604396 frameshift variant C/CGC in-del 2
rs1057518800 1.000 0.036 12 13567228 missense variant C/T snp 2
rs1057518801 0.923 0.107 2 165130238 missense variant A/G snp 2
rs752390804 0.923 0.036 16 28873554 missense variant G/A snp 2
rs1057518777 1.000 0.036 15 25339239 frameshift variant A/AGTATGAGATGTAG in-del 2
rs751569508 1.000 0.036 17 16194473 missense variant G/A snp 2.5E-05 1