Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 55
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 42
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 23
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 23
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 22
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 19
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 19
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 15
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 14
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 7
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 7
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 7
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 7
rs397507548
PTPN11
0.851 0.160 12 112489093 missense variant A/C snv 6
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 5
rs1057519819
MAP2K1
0.851 0.240 15 66436750 missense variant T/C snv 5
rs768366978
NF1
0.851 0.240 17 31352411 missense variant C/T snv 4.0E-06 5
rs866445127
NF1
0.851 0.240 17 31352348 stop gained C/T snv 5
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 5
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 5
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 5
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 5
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 5
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 5
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 4