NRGN, neurogranin, 4900

N. diseases: 69; N. variants: 4
Disease: Child Development Disorders, Pervasive ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs55661361
rs55661361 		1.000 0.040 11 124744061 intron variant G/A snv 0.43
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 2 2017 2019