Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852812
rs137852812
SOS1
4 0.851 0.200 2 39051211 missense variant G/T snv 0.800 1.000 9 2007 2011
dbSNP: rs137852813
rs137852813
SOS1
11 0.807 0.200 2 39051202 missense variant A/C;G snv 0.800 1.000 9 2007 2011
dbSNP: rs137852814
rs137852814
SOS1
16 0.752 0.240 2 39022774 missense variant T/A;C snv 4.0E-06 0.800 1.000 9 2007 2011
dbSNP: rs267607079
rs267607079
SOS1
13 0.776 0.240 2 39022772 missense variant C/A;G snv 0.800 1.000 9 2007 2011
dbSNP: rs267607080
rs267607080
SOS1
2 0.925 0.160 2 39023134 missense variant A/G snv 0.800 1.000 9 2007 2011
dbSNP: rs397517159
rs397517159
SOS1
4 0.882 0.200 2 39007168 missense variant C/T snv 0.800 1.000 9 2007 2011
dbSNP: rs397517149
rs397517149
SOS1
4 0.851 0.200 2 39022786 missense variant T/G snv 0.800 1.000 8 2007 2011
dbSNP: rs1367714753
rs1367714753
SOS1
1 1.000 0.160 2 39006522 missense variant G/C snv 0.700 1.000 8 2007 2011
dbSNP: rs142094234
rs142094234
SOS1
1 1.000 0.160 2 39051253 missense variant A/G snv 8.4E-05 2.8E-05 0.700 1.000 8 2007 2011
dbSNP: rs1431574387
rs1431574387
SOS1
1 1.000 0.160 2 39022984 missense variant C/G snv 7.0E-06 0.700 1.000 8 2007 2011
dbSNP: rs1553362937
rs1553362937
SOS1
1 1.000 0.160 2 39058713 missense variant G/C snv 0.700 1.000 8 2007 2011
dbSNP: rs371314838
rs371314838
SOS1
2 0.925 0.160 2 39022938 missense variant C/T snv 5.6E-05 3.5E-05 0.700 1.000 8 2007 2011
dbSNP: rs397517147
rs397517147
SOS1
3 0.882 0.200 2 39023131 missense variant C/T snv 4.0E-06 0.700 1.000 8 2007 2011
dbSNP: rs397517148
rs397517148
SOS1
27 0.776 0.200 2 39023128 missense variant C/T snv 0.700 1.000 8 2007 2011
dbSNP: rs397517150
rs397517150
SOS1
7 0.827 0.160 2 39023118 missense variant A/C;G snv 0.700 1.000 8 2007 2011
dbSNP: rs397517153
rs397517153
SOS1
2 0.925 0.160 2 39022779 missense variant A/C;G snv 4.0E-06 0.700 1.000 8 2007 2011
dbSNP: rs397517154
rs397517154
SOS1
16 0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 8 2007 2011
dbSNP: rs397517164
rs397517164
SOS1
2 0.925 0.160 2 39058696 missense variant C/T snv 0.700 1.000 8 2007 2011
dbSNP: rs397517166
rs397517166
SOS1
2 0.925 0.160 2 39058683 missense variant G/C snv 0.700 1.000 8 2007 2011
dbSNP: rs397517172
rs397517172
SOS1
3 0.925 0.160 2 39056704 missense variant T/C snv 0.700 1.000 8 2007 2011
dbSNP: rs397517180
rs397517180
SOS1
2 0.925 0.160 2 39035440 missense variant C/A snv 0.700 1.000 8 2007 2011
dbSNP: rs574088829
rs574088829
SOS1
2 0.925 0.160 2 39012319 missense variant T/A;G snv 4.0E-06 0.700 1.000 8 2007 2011
dbSNP: rs397517156
rs397517156
SOS1
4 0.851 0.200 2 39012333 missense variant T/A snv 0.700 0
dbSNP: rs724160007
rs724160007
SOS1
1 1.000 0.160 2 39035276 missense variant T/C snv 2.4E-05 0.700 0
dbSNP: rs727504295
rs727504295
SOS1
2 0.925 0.160 2 39023106 missense variant C/T snv 0.700 0