Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 8
rs397507548
PTPN11
0.851 0.160 12 112489093 missense variant A/C snv 6
rs397509343
BRAF
1.000 0.160 7 140801531 missense variant A/C snv 1
rs727505093
SOS1
1.000 0.160 2 39014838 missense variant A/C snv 1
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 13
rs137852813
SOS1
0.807 0.200 2 39051202 missense variant A/C;G snv 11
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 7
rs397517174
SOS1
0.925 0.160 2 39054822 missense variant A/C;G snv 3
rs397516903
BRAF
0.925 0.200 7 140801533 missense variant A/C;G snv 2
rs397517153
SOS1
0.925 0.160 2 39022779 missense variant A/C;G snv 4.0E-06 2
rs730881014
RIT1
0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs397507505
PTPN11
0.827 0.240 12 112450352 missense variant A/C;G;T snv 5
rs397516830
RAF1
0.827 0.160 3 12604182 missense variant A/C;G;T snv 5
rs869025194
RIT1
0.882 0.280 1 155904496 missense variant A/C;G;T snv 4
rs3730271
RAF1
1.000 0.160 3 12604195 missense variant A/C;G;T snv 1
rs397517042
KRAS
0.925 0.200 12 25209896 missense variant A/C;T snv 2
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 15
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 14
rs397507547
PTPN11
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06 14
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 5