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: rs745997770
rs745997770
2 0.925 0.120 1 197102323 stop gained G/A snv 4.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs765275884
rs765275884
2 0.925 0.120 1 197143279 frameshift variant AT/- delins 0.700 1.000 1 2018 2018
dbSNP: rs1558005340
rs1558005340
4 0.851 0.280 1 160127638 frameshift variant C/- del 0.700 1.000 1 2020 2020
dbSNP: rs1558008455
rs1558008455
4 0.851 0.280 1 160135284 frameshift variant GT/- delins 0.700 1.000 1 2020 2020
dbSNP: rs1556405129
rs1556405129
DCX
2 0.925 0.080 X 111410209 missense variant A/T snv 0.700 1.000 1 2018 2018
dbSNP: rs104894780
rs104894780
DCX
3 0.882 0.120 X 111401121 missense variant G/A 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: rs104894784
rs104894784
DCX
2 0.925 0.080 X 111410166 missense variant C/A;T snv 0.700 0
dbSNP: rs104894785
rs104894785
DCX
2 0.925 0.080 X 111410134 stop gained G/A;C 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: rs201870761
rs201870761
DCX
1 1.000 0.080 X 111410089 missense variant T/A;C snv 5.5E-06 0.700 0
dbSNP: rs267606317
rs267606317
DCX
1 1.000 0.080 X 111410094 missense variant C/T snv 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
dbSNP: rs587783518
rs587783518
DCX
1 1.000 0.080 X 111301745 splice acceptor variant T/C snv 0.700 0
dbSNP: rs587783519
rs587783519
DCX
1 1.000 0.080 X 111410284 stop gained G/A snv 0.700 0
dbSNP: rs587783520
rs587783520
DCX
1 1.000 0.080 X 111410275 frameshift variant T/- delins 0.700 0
dbSNP: rs587783521
rs587783521
DCX
2 0.925 0.080 X 111410271 missense variant A/G snv 0.700 0
dbSNP: rs587783522
rs587783522
DCX
1 1.000 0.080 X 111410269 stop gained G/A snv 0.700 0
dbSNP: rs587783523
rs587783523
DCX
2 0.925 0.080 X 111410249 missense variant C/A snv 0.700 0
dbSNP: rs587783524
rs587783524
DCX
1 1.000 0.080 X 111410245 frameshift variant TCTT/- delins 0.700 0
dbSNP: rs587783525
rs587783525
DCX
1 1.000 0.080 X 111410232 missense variant C/G snv 0.700 0
dbSNP: rs587783526
rs587783526
DCX
1 1.000 0.080 X 111410229 missense variant A/C snv 0.700 0
dbSNP: rs587783527
rs587783527
DCX
1 1.000 0.080 X 111410217 missense variant C/T snv 0.700 0
dbSNP: rs587783528
rs587783528
DCX
1 1.000 0.080 X 111410214 missense variant T/C snv 0.700 0
dbSNP: rs587783529
rs587783529
DCX
1 1.000 0.080 X 111410212 missense variant G/A snv 0.700 0