Source: CURATED

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: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0376480
Disease: Gingival Overgrowth
Gingival Overgrowth
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0234376
Disease: Action Tremor
Action Tremor
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C1866231
Disease: Full cheeks
Full cheeks
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0026837
Disease: Muscle Rigidity
Muscle Rigidity
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
BLEPHAROSPASM, BENIGN ESSENTIAL, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C4317146
Disease: Acid reflux
Acid reflux
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0700292
Disease: Hypoxemia
Hypoxemia
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C1849683
Disease: No social interaction
No social interaction
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C4021975
Disease: Abnormality of the tonsils
Abnormality of the tonsils
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C4022919
Disease: Appendicular hypotonia
Appendicular hypotonia
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.700 0
dbSNP: rs878853250
rs878853250
0.752 0.360 12 51699663 stop gained T/A;C snv
CUI: C0476273
Disease: Respiratory distress
Respiratory distress
0.700 0