Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516829
RAF1
1.000 0.160 3 12604184 missense variant A/T snv 1
rs587782971
RAF1
1.000 0.160 3 12608895 missense variant A/G snv 1
rs587782972
RAF1
1.000 0.160 3 12591729 missense variant C/A snv 1
rs727503384
RAF1
1.000 0.160 3 12611985 missense variant G/C snv 1
rs730881003
RAF1
1.000 0.160 3 12585794 missense variant A/G snv 1
rs869025190
RIT1
1.000 0.160 1 155910462 missense variant C/A snv 1
rs869025192
RIT1
1.000 0.160 1 155904499 missense variant C/G snv 1
rs869025196
RIT1
1.000 0.160 1 155904489 missense variant G/A snv 7.0E-06 1
rs368625677
RRAS
1.000 0.160 19 49637121 missense variant C/G;T snv 4.1E-06; 3.3E-05 1
rs1553353452
SOS1
1.000 0.160 2 39007033 missense variant C/T snv 1
rs397517146
SOS1
1.000 0.160 2 39024080 missense variant T/C snv 1
rs397517163
SOS1
1.000 0.160 2 38996981 missense variant A/G snv 1
rs727505093
SOS1
1.000 0.160 2 39014838 missense variant A/C snv 1
rs180177036
BRAF
0.925 0.200 7 140778053 missense variant C/A;G snv 2
rs397507477
BRAF
1.000 0.160 7 140777995 missense variant G/A snv 2
rs397516903
BRAF
0.925 0.200 7 140801533 missense variant A/C;G snv 2
rs397516904
BRAF
0.925 0.200 7 140801487 missense variant T/C;G snv 2
rs727502904
BRAF
0.925 0.200 7 140734763 missense variant G/A;T snv 2
rs727504375
BRAF
0.925 0.200 7 140778059 missense variant T/G snv 2
rs1441638629
GH1 ; CSHL1
0.925 0.200 17 63918773 missense variant C/T snv 4.0E-06 1.4E-05 2
rs1434040739
HRAS ; LOC101059906 ; LRRC56
0.925 0.200 11 532745 missense variant T/A snv 8.1E-06 7.0E-06 2
rs745410279
IGF1
0.925 0.200 12 102478498 missense variant T/C snv 4.1E-06 2
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 2
rs193929331
KRAS
0.925 0.160 12 25245372 missense variant T/C snv 2
rs202247812
KRAS
1.000 0.160 12 25225717 missense variant T/C snv 2