Disease: Chronic Lymphocytic Leukemia
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519959
SF3B2
0.882 0.200 11 66063028 missense variant A/C snv 4
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 5
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 7
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 8
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22