Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397517149
SOS1
0.851 0.200 2 39022786 missense variant T/G snv 4
rs397517156
SOS1
0.851 0.200 2 39012333 missense variant T/A snv 4
rs397517159
SOS1
0.882 0.200 2 39007168 missense variant C/T snv 4
rs397517147
SOS1
0.882 0.200 2 39023131 missense variant C/T snv 4.0E-06 3
rs397517172
SOS1
0.925 0.160 2 39056704 missense variant T/C snv 3
rs397517174
SOS1
0.925 0.160 2 39054822 missense variant A/C;G snv 3
rs267607080
SOS1
0.925 0.160 2 39023134 missense variant A/G snv 2
rs397517153
SOS1
0.925 0.160 2 39022779 missense variant A/C;G snv 4.0E-06 2
rs397517164
SOS1
0.925 0.160 2 39058696 missense variant C/T snv 2
rs397517166
SOS1
0.925 0.160 2 39058683 missense variant G/C snv 2
rs397517180
SOS1
0.925 0.160 2 39035440 missense variant C/A snv 2
rs727504295
SOS1
0.925 0.160 2 39023106 missense variant C/T snv 2
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
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs397516827
RAF1
0.882 0.160 3 12604194 missense variant G/A;C;T snv 9
rs80338797
RAF1
0.827 0.160 3 12584624 missense variant G/C;T snv 7
rs121434594
RAF1
0.827 0.160 3 12604189 missense variant G/A;C;T snv 5
rs397516830
RAF1
0.827 0.160 3 12604182 missense variant A/C;G;T snv 5
rs397516813
RAF1
0.925 0.160 3 12599717 missense variant C/G snv 3
rs727505017
RAF1
0.882 0.200 3 12604201 missense variant A/G;T snv 3
rs80338799
RAF1
0.882 0.160 3 12585745 missense variant G/A;C snv 3
rs397516815
RAF1
0.925 0.160 3 12585760 missense variant T/C snv 2