rs11866328, GRIN2A

N. diseases: 3
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.
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.925 0.120 16 9768699 intron variant G/T snv 0.38 0.810 1.000 1 2011 2011
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.925 0.120 16 9768699 intron variant G/T snv 0.38 0.700 1.000 1 2013 2013
Bradykinesia
CUI: C0233565
Disease: Bradykinesia
16 0.925 0.120 16 9768699 intron variant G/T snv 0.38 0.010 1.000 1 2012 2012