Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs2279115
BCL2
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 14
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
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
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 6
rs4353229
CASP7
0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs859
STARD5 ; IL16
0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6