COMT, catechol-O-methyltransferase, 1312

N. diseases: 622; N. variants: 47
Disease: Schizophrenia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9332377
rs9332377
Entrez Id: 421;1312
Gene Symbol: ARVCF;COMT
ARVCF;COMT
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE Eight SNPs were nominally associated with SZ in either case-control or family based analyses (p < 0.05, rs7631540 and rs2046496 in DRD3; rs363399 and rs10082463 in SLC18A2; rs4680, rs4646315 and rs9332377 in COMT). rs6271 at DBH was associated in both analyses. 23932573 2013