Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs559063155
SF3B1
0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 1
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 16
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 8
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 7
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs1057519961
SF3B1
0.851 0.240 2 197402759 missense variant C/T snv 4
rs775623976
SF3B1
0.851 0.240 2 197402760 missense variant G/A;C snv 4.0E-06 4
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs1057519959
SF3B2
0.882 0.200 11 66063028 missense variant A/C snv 4
rs587781894
ATM ; C11orf65
0.882 0.360 11 108365360 missense variant G/A;C snv 8.0E-06 7.0E-06 3
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 1
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 1
rs755415626
SF3B1
0.925 0.200 2 197401887 missense variant C/T snv 7.0E-06 2
rs1057519831
PLCG2
1.000 0.120 16 81912655 missense variant C/T snv 1
rs1057519832
PLCG2
1.000 0.120 16 81928578 missense variant A/C;G;T snv 1