Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs20576
TNFRSF10A
0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs563378859
TP53
0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 8
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 7
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 7
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs1392080411
KLF2
0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06 5
rs6083471 0.882 0.240 20 24274115 intergenic variant T/C snv 2.8E-02 3
rs604714
DPAGT1
0.925 0.120 11 119099986 intron variant C/A snv 0.31 3
rs80351309
LOC105374370
0.882 0.240 4 7076231 regulatory region variant C/T snv 1.1E-03 3