Disease: Chronic Lymphocytic Leukemia
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519959
SF3B2
0.882 0.200 11 66063028 missense variant A/C snv 4
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
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
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
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 17
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
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
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5