Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C4021152
Disease: Abnormal CNS myelination
Abnormal CNS myelination
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C4317146
Disease: Acid reflux
Acid reflux
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
Aplasia/Hypoplasia involving the central nervous system
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
Aplasia/Hypoplasia of the corpus callosum
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0345326
Disease: Congenital phimosis
Congenital phimosis
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C4021758
Disease: Delayed CNS myelination
Delayed CNS myelination
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0013132
Disease: Drooling
Drooling
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0014877
Disease: Esotropia
Esotropia
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C1854780
Disease: Flaring of rib cage
Flaring of rib cage
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C1857280
Disease: Infra-orbital crease
Infra-orbital crease
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding)
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C3150077
Disease: Mild short stature
Mild short stature
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk
0.700 0
dbSNP: rs267606826
rs267606826
0.708 0.520 14 28767903 stop gained C/A;G;T snv
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.700 0