rs774843232, PGAP2

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.
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 17
CUI: C3280153
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 17
6 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.800 0
Absence Seizures
CUI: C4316903
Disease: Absence Seizures
8 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.700 0
Brain atrophy
CUI: C4551584
Disease: Brain atrophy
46 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.700 0
Delayed speech and language development
CUI: C0454644
Disease: Delayed speech and language development
192 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.700 0
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.700 0
Motor delay
CUI: C1854301
Disease: Motor delay
34 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.700 0
Neonatal Hypotonia
CUI: C2267233
Disease: Neonatal Hypotonia
45 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.700 0
Serum alkaline phosphatase raised
CUI: C1314665
Disease: Serum alkaline phosphatase raised
6 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.700 0
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 0.010 1.000 1 2013 2013