Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs267606920
NRAS
0.882 0.160 1 114713911 missense variant C/T snv 7.0E-06 1
rs267606921
NRAS
0.882 0.160 1 114713941 missense variant G/A snv 1
rs672601334
RIT1
0.752 0.400 1 155904798 missense variant G/C snv 1
rs672601335
RIT1
0.882 0.160 1 155904456 missense variant C/G snv 1
rs869025193
RIT1
0.925 0.160 1 155904498 missense variant T/C snv 1
rs137852812
SOS1
0.851 0.200 2 39051211 missense variant G/T snv 1
rs137852813
SOS1
0.807 0.200 2 39051202 missense variant A/C;G snv 1
rs137852814
SOS1
0.752 0.240 2 39022774 missense variant T/A;C snv 4.0E-06 1
rs267607079
SOS1
0.776 0.240 2 39022772 missense variant C/A;G snv 1
rs267607080
SOS1
0.925 0.160 2 39023134 missense variant A/G snv 1
rs397517147
SOS1
0.882 0.200 2 39023131 missense variant C/T snv 4.0E-06 1
rs397517148
SOS1
0.776 0.200 2 39023128 missense variant C/T snv 1
rs397517149
SOS1
0.851 0.200 2 39022786 missense variant T/G snv 1
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 1
rs397517153
SOS1
0.925 0.160 2 39022779 missense variant A/C;G snv 4.0E-06 1
rs397517154
SOS1
0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 1
rs397517159
SOS1
0.882 0.200 2 39007168 missense variant C/T snv 1
rs397517164
SOS1
0.925 0.160 2 39058696 missense variant C/T snv 1
rs397517166
SOS1
0.925 0.160 2 39058683 missense variant G/C snv 1
rs397517172
SOS1
0.925 0.160 2 39056704 missense variant T/C snv 1
rs397517180
SOS1
0.925 0.160 2 39035440 missense variant C/A snv 1
rs727504295
SOS1
0.925 0.160 2 39023106 missense variant C/T snv 1
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 2