rs1557781252, GATAD2B

N. diseases: 33
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
0.700 CausalMutation CLINVAR
Induced vaginal delivery
CUI: C4072908
Disease: Induced vaginal delivery
0.700 CausalMutation CLINVAR
Polyhydramnios
CUI: C0020224
Disease: Polyhydramnios
0.700 CausalMutation CLINVAR
Prominent forehead
CUI: C1837260
Disease: Prominent forehead
0.700 CausalMutation CLINVAR
Low set ears
CUI: C0239234
Disease: Low set ears
0.700 CausalMutation CLINVAR
Fecal Incontinence
CUI: C0015732
Disease: Fecal Incontinence
0.700 CausalMutation CLINVAR
Large head (disorder)
CUI: C2243051
Disease: Large head (disorder)
0.700 CausalMutation CLINVAR
Orbital separation excessive
CUI: C0020534
Disease: Orbital separation excessive
0.700 CausalMutation CLINVAR
Abnormal delivery
CUI: C0549629
Disease: Abnormal delivery
0.700 CausalMutation CLINVAR
Poor suck
CUI: C1837142
Disease: Poor suck
0.700 CausalMutation CLINVAR
Chronic diarrhea
CUI: C0401151
Disease: Chronic diarrhea
0.700 CausalMutation CLINVAR
Growth delay
CUI: C0456070
Disease: Growth delay
0.700 CausalMutation CLINVAR
Microstomia
CUI: C0026034
Disease: Microstomia
0.700 CausalMutation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 CausalMutation CLINVAR
Neonatal hypoglycemia
CUI: C0158986
Disease: Neonatal hypoglycemia
0.700 CausalMutation CLINVAR
Pediatric failure to thrive
CUI: C2315100
Disease: Pediatric failure to thrive
0.700 CausalMutation CLINVAR
Generalized hypotonia
CUI: C1858120
Disease: Generalized hypotonia
0.700 CausalMutation CLINVAR
Thin upper lip vermilion
CUI: C1865017
Disease: Thin upper lip vermilion
0.700 CausalMutation CLINVAR
Urinary Incontinence
CUI: C0042024
Disease: Urinary Incontinence
0.700 CausalMutation CLINVAR
Gait imbalance
CUI: C1836150
Disease: Gait imbalance
0.700 CausalMutation CLINVAR
Broad-based gait
CUI: C0856863
Disease: Broad-based gait
0.700 CausalMutation CLINVAR
Chronic constipation
CUI: C0401149
Disease: Chronic constipation
0.700 CausalMutation CLINVAR
Macrocephaly at birth
CUI: C1836599
Disease: Macrocephaly at birth
0.700 CausalMutation CLINVAR
Exotropia
CUI: C0015310
Disease: Exotropia
0.700 CausalMutation CLINVAR
Delayed bone age
CUI: C0541764
Disease: Delayed bone age
0.700 CausalMutation CLINVAR