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: rs165774
rs165774
0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27
CUI: C0184567
Disease: Acute onset pain
Acute onset pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs4680
rs4680
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44
CUI: C0184567
Disease: Acute onset pain
Acute onset pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs6269
rs6269
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38
CUI: C0184567
Disease: Acute onset pain
Acute onset pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017