Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0549629
Disease:
Abnormal delivery
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1837142
Disease:
Poor suck
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0401151
Disease:
Chronic diarrhea
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0456070
Disease:
Growth delay
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0026034
Disease:
Microstomia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0557874
Disease:
Global developmental delay
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0158986
Disease:
Neonatal hypoglycemia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C2315100
Disease:
Pediatric failure to thrive
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1858120
Disease:
Generalized hypotonia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1865017
Disease:
Thin upper lip vermilion
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0042024
Disease:
Urinary Incontinence
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1836150
Disease:
Gait imbalance
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0856863
Disease:
Broad-based gait
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0401149
Disease:
Chronic constipation
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1836599
Disease:
Macrocephaly at birth
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0015310
Disease:
Exotropia
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0541764
Disease:
Delayed bone age
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C4022873
Disease:
Small pituitary gland
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C4317146
Disease:
Acid reflux
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C4023678
Disease:
Monocular strabismus
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0003079
Disease:
Anisocoria
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1142533
Disease:
Smooth philtrum
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1854882
Disease:
Absent speech
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0332615
Disease:
Myopathic facies
A 0.700 CausalMutation CLINVAR