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: rs778148267
rs778148267
NFKB2
1 1.000 0.080 10 102400738 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2017 2017
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: 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: rs587783522
rs587783522
DCX
1 1.000 0.080 X 111410269 stop gained G/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
dbSNP: rs587783530
rs587783530
DCX
1 1.000 0.080 X 111410208 missense variant T/C snv 0.700 0
dbSNP: rs587783531
rs587783531
DCX
1 1.000 0.080 X 111410204 missense variant G/A;T snv 0.700 0
dbSNP: rs587783532
rs587783532
DCX
1 1.000 0.080 X 111410189 stop gained G/T snv 0.700 0
dbSNP: rs587783533
rs587783533
DCX
1 1.000 0.080 X 111410181 missense variant G/A snv 0.700 0
dbSNP: rs587783535
rs587783535
DCX
1 1.000 0.080 X 111410167 missense variant G/A snv 0.700 0
dbSNP: rs587783536
rs587783536
DCX
1 1.000 0.080 X 111410127 missense variant A/G snv 0.700 0
dbSNP: rs587783538
rs587783538
DCX
1 1.000 0.080 X 111410100 missense variant C/A;T snv 0.700 0
dbSNP: rs587783539
rs587783539
DCX
1 1.000 0.080 X 111410397 start lost A/G snv 0.700 0
dbSNP: rs587783540
rs587783540
DCX
1 1.000 0.080 X 111410098 missense variant C/T snv 0.700 0
dbSNP: rs587783541
rs587783541
DCX
1 1.000 0.080 X 111410095 missense variant G/A;C snv 0.700 0
dbSNP: rs587783542
rs587783542
DCX
1 1.000 0.080 X 111410062 missense variant T/A snv 0.700 0
dbSNP: rs587783544
rs587783544
DCX
1 1.000 0.080 X 111410035 missense variant C/T snv 0.700 0