PRRC2A, proline rich coiled-coil 2A, 7916

N. diseases: 45; N. variants: 32
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: rs115052633
rs115052633 		1.000 0.040 6 31621487 intron variant C/G;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017