Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554401434
rs1554401434
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4014435
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
ACGCCC 0.700 CausalMutation CLINVAR
dbSNP: rs1554480537
rs1554480537
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4014435
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
T 0.700 CausalMutation CLINVAR
dbSNP: rs1563183469
rs1563183469
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0000772
Disease:
Multiple congenital anomalies
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183469
rs1563183469
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4014435
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183469
rs1563183469
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0175754
Disease:
Agenesis of corpus callosum
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0020505
Disease:
Hyperphagia
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0549629
Disease:
Abnormal delivery
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0454642
Disease:
Receptive language delay
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C1843367
Disease:
Poor school performance
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4054546
Disease:
Melanocortin 4 Receptor Deficiency
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0557874
Disease:
Global developmental delay
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0016873
Disease:
Fused Teeth
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4072903
Disease:
Primary Caesarian section
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0034194
Disease:
Pyloric Stenosis
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0565599
Disease:
Maternal hypertension
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4317146
Disease:
Acid reflux
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4014435
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C1855925
Disease:
Hyperopia, High
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0152423
Disease:
Congenital small ears
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C2243051
Disease:
Large head (disorder)
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0004352
Disease:
Autistic Disorder
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C2315100
Disease:
Pediatric failure to thrive
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C1837142
Disease:
Poor suck
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0266610
Disease:
Preauricular dimple
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0020534
Disease:
Orbital separation excessive
T 0.700 GeneticVariation CLINVAR