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: rs1057518667
rs1057518667
SCN8A
1 1.000 0.160 12 51789402 missense variant A/G snv 0.700 0
dbSNP: rs1057519540
rs1057519540
SCN8A
2 0.925 0.160 12 51768895 missense variant A/G snv 0.700 0
dbSNP: rs1057519557
rs1057519557
SCN8A
1 1.000 0.160 12 51699783 missense variant A/G snv 0.700 0
dbSNP: rs1057524820
rs1057524820
SCN8A
33 0.776 0.280 12 51765746 missense variant G/A;T snv 0.700 0
dbSNP: rs1064793263
rs1064793263
SCN8A
1 1.000 0.160 12 51790404 missense variant G/A snv 0.700 0
dbSNP: rs1064794727
rs1064794727
SCN8A
3 0.882 0.160 12 51807092 missense variant T/C snv 0.700 0
dbSNP: rs1135401806
rs1135401806
SCN8A
1 1.000 0.160 12 51789393 missense variant A/T snv 0.700 0
dbSNP: rs1555225794
rs1555225794
SCN8A
1 1.000 0.160 12 51765729 missense variant T/C snv 0.700 0
dbSNP: rs1555228771
rs1555228771
SCN8A
1 1.000 0.160 12 51789408 missense variant A/C snv 0.700 0
dbSNP: rs1555231012
rs1555231012
SCN8A
1 1.000 0.160 12 51806765 missense variant T/C snv 0.700 0
dbSNP: rs761386688
rs761386688
SCN8A
1 1.000 0.160 12 51769230 missense variant C/A snv 1.6E-05 0.700 0
dbSNP: rs796053216
rs796053216
SCN8A
4 0.851 0.160 12 51790401 stop gained G/A;T snv 0.700 0
dbSNP: rs869312690
rs869312690
SCN8A
3 0.925 0.240 12 51806762 missense variant A/G snv 0.700 0
dbSNP: rs886044328
rs886044328
SCN8A
3 0.882 0.160 12 51806363 missense variant G/A snv 0.700 0
dbSNP: rs202151337
rs202151337
SCN8A
4 0.925 0.160 12 51806788 missense variant A/G snv 0.700 1.000 1 2012 2012
dbSNP: rs863225295
rs863225295
SCN8A
1 1.000 0.160 12 51765801 missense variant T/G snv 0.700 1.000 1 2013 2013
dbSNP: rs879255694
rs879255694
SCN8A
1 1.000 0.160 12 51688784 missense variant G/A snv 0.700 1.000 1 2013 2013
dbSNP: rs879255701
rs879255701
SCN8A
1 1.000 0.160 12 51765750 missense variant T/A snv 0.700 1.000 1 2013 2013
dbSNP: rs797045013
rs797045013
SCN8A
2 0.925 0.160 12 51751523 missense variant C/T snv 0.700 1.000 2 2013 2014
dbSNP: rs758253791
rs758253791
SCN8A
1 1.000 0.160 12 51745907 missense variant C/T snv 1.4E-05 7.1E-06 0.700 1.000 1 2014 2014
dbSNP: rs796053228
rs796053228
SCN8A
4 0.882 0.160 12 51807100 missense variant C/G;T snv 0.700 1.000 3 2014 2015
dbSNP: rs879255695
rs879255695
SCN8A
1 1.000 0.160 12 51688786 missense variant A/G snv 0.700 1.000 2 2015 2015
dbSNP: rs761336234
rs761336234
SCN8A
1 1.000 0.160 12 51706668 missense variant C/T snv 2.2E-05 4.9E-05 0.700 1.000 1 2015 2015
dbSNP: rs796053217
rs796053217
SCN8A
1 1.000 0.160 12 51790413 missense variant A/G snv 0.700 1.000 1 2015 2015
dbSNP: rs796053229
rs796053229
SCN8A
3 0.882 0.160 12 51807101 missense variant G/A;T snv 4.0E-06 0.700 1.000 1 2015 2015