rs2189814, GRM3

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.
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.925 0.040 7 86702440 intron variant T/A;C snv 0.010 1.000 1 2011 2011
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.925 0.040 7 86702440 intron variant T/A;C snv 0.010 1.000 1 2011 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.925 0.040 7 86702440 intron variant T/A;C snv 0.010 1.000 1 2011 2011