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: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.100 0.854 123 1997 2019
dbSNP: rs165599
rs165599
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.100 0.727 11 2004 2018
dbSNP: rs737865
rs737865
0.763 0.240 22 19942598 intron variant A/G snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.090 0.889 9 2004 2017
dbSNP: rs749437638
rs749437638
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.050 1.000 5 2008 2017
dbSNP: rs165774
rs165774
0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.040 1.000 4 2011 2017
dbSNP: rs6267
rs6267
0.827 0.200 22 19962740 missense variant G/A;T snv 4.8E-05; 1.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.040 1.000 4 2005 2011
dbSNP: rs2075507
rs2075507
0.925 0.040 22 19940569 intron variant G/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 0.500 2 2007 2009
dbSNP: rs4818
rs4818
0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 0.500 2 2016 2018
dbSNP: rs1445081098
rs1445081098
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs165655
rs165655
1.000 0.040 22 19970240 3 prime UTR variant G/A snv 0.56
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs165656
rs165656
0.925 0.200 22 19961340 intron variant G/A;C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 < 0.001 1 2011 2011
dbSNP: rs165688
rs165688
1.000 0.040 22 19963748 missense variant G/A snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2004 2004
dbSNP: rs2020917
rs2020917
0.851 0.160 22 19941361 intron variant C/T snv 0.22
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs2097603
rs2097603
0.882 0.040 22 19940569 intron variant G/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs4633
rs4633
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs755245483
rs755245483
1.000 0.040 22 19963750 synonymous variant G/A;T snv 4.0E-06
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs9332377
rs9332377
0.882 0.120 22 19968169 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2013 2013