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: rs104894779
rs104894779
DCX
2 0.925 0.120 X 111410215 missense variant C/T snv 0.700 0
dbSNP: rs104894780
rs104894780
DCX
3 0.882 0.120 X 111401121 missense variant G/A snv 0.700 0
dbSNP: rs104894781
rs104894781
DCX
2 0.925 0.120 X 111401322 missense variant A/G snv 0.700 0
dbSNP: rs104894782
rs104894782
DCX
3 0.882 0.120 X 111401087 missense variant G/C;T snv 0.700 0
dbSNP: rs104894783
rs104894783
DCX
2 0.925 0.120 X 111410260 missense variant T/G snv 0.700 0
dbSNP: rs104894786
rs104894786
DCX
2 0.925 0.120 X 111410188 missense variant C/A snv 0.700 0
dbSNP: rs122457137
rs122457137
DCX
3 0.882 0.120 X 111410223 missense variant C/A;T snv 0.700 0
dbSNP: rs1556401725
rs1556401725
DCX
1 1.000 0.120 X 111400989 splice donor variant C/- delins 0.700 0
dbSNP: rs1556401744
rs1556401744
DCX
2 0.925 0.120 X 111401010 frameshift variant AG/- delins 0.700 0
dbSNP: rs1556404991
rs1556404991
DCX
1 1.000 0.120 X 111410043 frameshift variant AG/- del 0.700 0
dbSNP: rs56030372
rs56030372
DCX
3 0.882 0.120 X 111401108 missense variant C/A;T snv 9.5E-06 0.700 0