Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518674
rs1057518674
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057521041
rs1057521041
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
T 0.700 CausalMutation CLINVAR
dbSNP: rs1131692164
rs1131692164
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
GACATC 0.700 CausalMutation CLINVAR
dbSNP: rs1131692165
rs1131692165
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
G 0.700 CausalMutation CLINVAR
dbSNP: rs1553187362
rs1553187362
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1553187443
rs1553187443
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553187446
rs1553187446
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
A 0.700 CausalMutation CLINVAR
dbSNP: rs1553188463
rs1553188463
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C3554448
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557778985
rs1557778985
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: C0042870
Disease:
Vitamin D Deficiency
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C4072908
Disease:
Induced vaginal delivery
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0020224
Disease:
Polyhydramnios
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C1837260
Disease:
Prominent forehead
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0239234
Disease:
Low set ears
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0015732
Disease:
Fecal Incontinence
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C2243051
Disease:
Large head (disorder)
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557781252
rs1557781252
Entrez Id: 57459
Gene Symbol: GATAD2B
GATAD2B
CUI: C0020534
Disease:
Orbital separation excessive
A 0.700 CausalMutation CLINVAR
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