rs165656, COMT

N. diseases: 5
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.
Arm Pain
CUI: C0239377
Disease: Arm Pain
6 0.925 0.200 22 19961340 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.925 0.200 22 19961340 intron variant G/A;C;T snv 0.010 1.000 1 2007 2007
Mental Retardation
CUI: C0025362
Disease: Mental Retardation
98 0.925 0.200 22 19961340 intron variant G/A;C;T snv 0.010 1.000 1 2007 2007
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.925 0.200 22 19961340 intron variant G/A;C;T snv 0.010 1 2011 2011
Temporomandibular Joint Disorders
CUI: C0039494
Disease: Temporomandibular Joint Disorders
25 0.925 0.200 22 19961340 intron variant G/A;C;T snv 0.010 1.000 1 2014 2014