Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 8
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 8
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 6
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs121913535
KRAS
0.742 0.320 12 25245348 missense variant C/A;G;T snv 5
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 4
rs121913428
EGFR
0.827 0.120 7 55174015 missense variant G/A;C snv 4
rs727502902
BRAF
0.882 0.080 7 140753338 inframe insertion -/TAG delins 4.0E-06 4
rs113994088
ALK
0.925 0.080 2 29222584 missense variant C/G snv 3
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 3
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 3
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 3
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 3
rs201744589
TP53
0.882 0.240 17 7673728 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 3
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 3
rs727503108
KRAS
0.882 0.280 12 25227345 missense variant C/A snv 4.0E-06 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 2
rs113994091
ALK
0.882 0.160 2 29222407 missense variant G/A;C snv 3.2E-05 2