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: rs165655
rs165655
Entrez Id: 421;1312
Gene Symbol: ARVCF;COMT
ARVCF;COMT
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE The PCR-based restriction fragment length polymorphism (PCR-RFLP) analysis was used to detect three single nucleotide polymorphisms (SNPs), rs165655 (A/G base change) and rs165815 (C/T base change) present in the ARVCF (armadillo repeat gene deletion in velocardiofacial syndrome) locus, and rs756656 (A/C base change) in the LOC128979 (expressed sequence tags, EST) locus, among 100 Chinese family trios consisting of fathers, mothers and affected offspring with schizophrenia. 15861775 2005