rs9879311, ATP2B2

N. diseases: 2
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.
Child Development Disorders, Pervasive
CUI: C0008074
Disease: Child Development Disorders, Pervasive
379 1.000 0.040 3 10373659 intron variant C/A;T snv 0.700 1.000 1 2017 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 1.000 0.040 3 10373659 intron variant C/A;T snv 0.700 1.000 1 2017 2017