Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10190751
CFLAR-AS1 ; CFLAR
0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042752
POU2AF1
0.925 0.120 11 111352386 3 prime UTR variant A/G snv 0.39 3
rs10494879
IL19
0.925 0.120 1 206778859 intron variant C/A;G snv 0.36 3
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 9
rs1057519833
EZH2
0.925 0.120 7 148809375 missense variant G/C snv 3
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11466782
ADAM19
0.925 0.120 5 157494947 intron variant A/G snv 0.10 3
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913105
FGFR3
0.653 0.600 4 1806163 missense variant A/C;T snv 30
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 18
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1257715362
MAPK10 ; ARHGAP24
0.925 0.120 4 85995065 missense variant A/G snv 7.0E-06 3
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1351687973
TP73
0.925 0.120 1 3731497 missense variant G/A snv 1.6E-05 3
rs1353428252
IDH2
0.851 0.120 15 90088681 missense variant A/C snv 8.0E-06 5
rs138228187
TIRAP
0.925 0.120 11 126292650 missense variant C/T snv 4.0E-05 1.4E-05 3
rs1555525126
TP53
0.925 0.120 17 7673749 missense variant T/C snv 3
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72