Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 3
rs104894104
CDKN2A
0.790 0.160 9 21971019 missense variant G/A;T snv 4
rs1057519908
MAP2K1
0.882 0.120 15 66435105 missense variant T/G snv 4
rs1057519910
MAP2K2
0.851 0.160 19 4117551 missense variant A/C;T snv 4
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 4
rs1057519948
RAC1
0.851 0.120 7 6387262 missense variant C/T snv 4
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
rs1057519959
SF3B2
0.882 0.200 11 66063028 missense variant A/C snv 4
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs1057519956
CNOT9
0.827 0.200 2 218583025 missense variant T/C snv 5
rs1057519957
CNOT9
0.827 0.200 2 218583026 missense variant C/G snv 5
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519757
PIK3R1
0.882 0.120 5 68293310 missense variant G/A;C snv 5
rs1057519841
PIK3R1
0.925 0.120 5 68295269 missense variant A/G snv 5
rs754688962
SF3B1
0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 6
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 6
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 6
rs770248150
KRAS
0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 6
rs1057519732
MAP2K1
0.827 0.160 15 66436824 missense variant C/A;T snv 6