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: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0011175
Disease: Dehydration
Dehydration
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0036572
Disease: Seizures
Seizures
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0020490
Disease: Hyperopia
Hyperopia
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0009806
Disease: Constipation
Constipation
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C1837142
Disease: Poor suck
Poor suck
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0018621
Disease: Hay fever
Hay fever
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0013362
Disease: Dysarthria
Dysarthria
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C4551520
Disease: Intention tremor
Intention tremor
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0375206
Disease: Hemiplegia/hemiparesis
Hemiplegia/hemiparesis
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0002418
Disease: Amblyopia
Amblyopia
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0038379
Disease: Strabismus
Strabismus
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0016202
Disease: Flatfoot
Flatfoot
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.700 0
dbSNP: rs1555745467
rs1555745467
0.752 0.240 19 13262771 missense variant C/A snv
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode
0.700 0