COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
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: rs4680
rs4680
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence
Chemically-Induced Disorders; Mental Disorders 0.040 1.000 4 2006 2013
dbSNP: rs9332377
rs9332377
0.882 0.120 22 19968169 intron variant C/A;T snv
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2010 2010