Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867830180
TNFRSF6B ; RTEL1 ; RTEL1-TNFRSF6B
0.925 0.120 20 63695147 missense variant G/A;T snv 3
rs8177400
TIRAP
0.882 0.160 11 126292695 missense variant G/A;C;T snv 2.8E-03; 1.2E-05 4
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs10190751
CFLAR-AS1 ; CFLAR
0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4
rs1351687973
TP73
0.925 0.120 1 3731497 missense variant G/A snv 1.6E-05 3
rs535311760
TP73
0.925 0.120 1 3730979 missense variant G/A snv 1.2E-05; 8.2E-06 3
rs867329357
ERCC5 ; BIVM-ERCC5
0.925 0.120 13 102872275 missense variant G/A snv 4.0E-06 4.9E-05 3
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs2274084
GJB2
0.882 0.240 13 20189503 missense variant C/T snv 5.4E-02 2.2E-02 6
rs138228187
TIRAP
0.925 0.120 11 126292650 missense variant C/T snv 4.0E-05 1.4E-05 3
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 9
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
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
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs10494879
IL19
0.925 0.120 1 206778859 intron variant C/A;G snv 0.36 3
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188