Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs587782177
TP53
0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs6104
SERPINB10 ; SERPINB2
0.807 0.160 18 63903295 missense variant C/G snv 0.29 0.28 6
rs439680 1.000 0.080 5 109998341 regulatory region variant C/G snv 3
rs12200782
BTN3A1
1.000 0.080 6 26402808 intron variant C/G snv 7.9E-02 1
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs116427960
HLA-B
0.925 0.120 6 31351449 intron variant C/G;T snv 3
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1138272
GSTP1
0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs402710
CLPTM1L
0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 18
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9