rs3753242, PRKCZ

N. diseases: 1
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.
Reasoning
CUI: C0684328
Disease: Reasoning
13 1 2138242 intron variant C/T snv 7.5E-02 0.700 1.000 1 2011 2011