rs1085308046, PTEN

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.
Arnold Chiari Malformation
CUI: C0003803
Disease: Arnold Chiari Malformation
4 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
Autistic behavior
CUI: C0856975
Disease: Autistic behavior
78 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
Hydrocephalus
CUI: C0020255
Disease: Hydrocephalus
37 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
Large head (disorder)
CUI: C2243051
Disease: Large head (disorder)
116 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
PTEN Hamartoma Tumor Syndrome
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
194 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
Senile angioma
CUI: C0343082
Disease: Senile angioma
2 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0
Social Communication Disorder
CUI: C0150080
Disease: Social Communication Disorder
4 0.790 0.240 10 87933160 missense variant T/C;G snv 0.700 0