COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Attention deficit hyperactivity disorder ×
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: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.100 0.950 20 2005 2017
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs2097603
rs2097603 		0.882 0.040 22 19940569 intron variant G/A;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs373611092
rs373611092 		0.925 0.160 22 19962794 missense variant A/G snv 8.4E-05 4.9E-05
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs4818
rs4818 		0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 < 0.001 1 2013 2013
dbSNP: rs740603
rs740603 		0.925 0.040 22 19957654 intron variant A/G snv 0.48
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2013 2013