rs11191582, NT5C2

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 10 103153896 intron variant G/A snv 7.7E-02 0.700 1.000 1 2017 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 0.700 1.000 1 2017 2017