rs1562171209, PHIP

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
Delayed speech and language development
192 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES
17 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
Feeding difficulties in infancy
CUI: C2674608
Disease: Feeding difficulties in infancy
22 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
Mild Mental Retardation
CUI: C0026106
Disease: Mild Mental Retardation
56 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
Neurodevelopmental delay
CUI: C4022738
Disease: Neurodevelopmental delay
24 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
Reduced concentration span
CUI: C0262630
Disease: Reduced concentration span
2 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
Sleep disturbances
CUI: C0037317
Disease: Sleep disturbances
74 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0
Specific learning disability
CUI: C4025790
Disease: Specific learning disability
13 0.851 0.160 6 79003821 missense variant T/C snv 0.700 0