rs1562171209, PHIP

N. diseases: 9
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sleep disturbances
CUI: C0037317
Disease: Sleep disturbances
0.700 GeneticVariation CLINVAR
Feeding difficulties in infancy
CUI: C2674608
Disease: Feeding difficulties in infancy
0.700 GeneticVariation CLINVAR
Neurodevelopmental delay
CUI: C4022738
Disease: Neurodevelopmental delay
0.700 GeneticVariation CLINVAR
Reduced concentration span
CUI: C0262630
Disease: Reduced concentration span
0.700 GeneticVariation CLINVAR
DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES
CUI: C4693860
Disease: DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES
0.700 GeneticVariation CLINVAR
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.700 GeneticVariation CLINVAR
Mild Mental Retardation
CUI: C0026106
Disease: Mild Mental Retardation
0.700 GeneticVariation CLINVAR
Delayed speech and language development
CUI: C0454644
Disease: Delayed speech and language development
0.700 GeneticVariation CLINVAR
Specific learning disability
CUI: C4025790
Disease: Specific learning disability
0.700 GeneticVariation CLINVAR