COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Unipolar Depression ×
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: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.100 1.000 11 2005 2019
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs174697
rs174697 		0.851 0.080 22 19966309 intron variant A/G snv 0.88
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs737865
rs737865 		0.763 0.240 22 19942598 intron variant A/G snv 0.23
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2011 2011