BCHE, butyrylcholinesterase, 590

N. diseases: 392; N. variants: 101
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1803274
rs1803274
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0085281
Disease:
Addictive Behavior
0.010 GeneticVariation BEFREE We report here the first investigation to be conducted on the status of BChE activity and the potential association of two BCHE gene SNPs, rs3495 (c.*189G > A) and rs1803274 (c.1699G>A, p.Ala567Thr, K-variant), with addiction vulnerability in heroin, hashish and polydrug users. 30707402 2019
dbSNP: rs3495
rs3495
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0085281
Disease:
Addictive Behavior
0.010 GeneticVariation BEFREE We report here the first investigation to be conducted on the status of BChE activity and the potential association of two BCHE gene SNPs, rs3495 (c.*189G > A) and rs1803274 (c.1699G>A, p.Ala567Thr, K-variant), with addiction vulnerability in heroin, hashish and polydrug users. 30707402 2019
dbSNP: rs1803274
rs1803274
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0002395
Disease:
Alzheimer's Disease
0.040 GeneticVariation BEFREE We found synergy between APOE-ε4 and SNPs localized in 5'UTR (rs1126680) and in intron 2 (rs55781031) of the BCHE-K allele (rs1803274) in 18% of patients with late-onset AD (n = 55). 30914707 2019
dbSNP: rs1803274
rs1803274
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0002395
Disease:
Alzheimer's Disease
0.040 GeneticVariation BEFREE Our interest in these mutations was initiated by studying the potential effects of the A539T substitution in the butyrylcholinesterase BChE-K variant on amyloid fibrils formation in Alzheimer's disease. 20060816 2010
dbSNP: rs1803274
rs1803274
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0002395
Disease:
Alzheimer's Disease
0.040 GeneticVariation BEFREE Polymorphisms of the butyrylcholinesterase gene (BCHE) are reported to associate with Alzheimer's disease and a recent study found a significant association of the BCHE K variant (G1615A/Ala539Thr) with Type 2 diabetes. 15258737 2004
dbSNP: rs1803274
rs1803274
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0002395
Disease:
Alzheimer's Disease
0.040 GeneticVariation BEFREE Dual activity structurally derived changes due to the A539T substitution can thus account for both neuroprotective characteristics caused by sustained acetylcholine levels and elevated AD risk due to inefficient interference with amyloidogenic processes. 19383604 2009
dbSNP: rs1126680
rs1126680
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE We found synergy between APOE-ε4 and SNPs localized in 5'UTR (rs1126680) and in intron 2 (rs55781031) of the BCHE-K allele (rs1803274) in 18% of patients with late-onset AD (n = 55). 30914707 2019
dbSNP: rs55781031
rs55781031
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE We found synergy between APOE-ε4 and SNPs localized in 5'UTR (rs1126680) and in intron 2 (rs55781031) of the BCHE-K allele (rs1803274) in 18% of patients with late-onset AD (n = 55). 30914707 2019
dbSNP: rs1799807
rs1799807
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0003578
Disease:
Apnea
0.020 GeneticVariation BEFREE People homozygous for the Asp70His mutation are expected to have prolonged apnoea in response to succinylcholine or mivacurium, similar to people with the Asp70Gly mutation. 11928765 2002
dbSNP: rs1799807
rs1799807
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C0003578
Disease:
Apnea
0.020 GeneticVariation BEFREE The clinically most important variant is atypical (D70G) BChE because people with this variant have 2 hours of apnea after receiving a dose of succinylcholine that is intended to paralyze muscles for 3-5 minutes. 10794391 2000
dbSNP: rs1799807
rs1799807
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1867468
Disease:
Apnea, Postanesthetic
C 0.700 CausalMutation CLINVAR
dbSNP: rs28933390
rs28933390
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C3889588
Disease:
BCHE, FLUORIDE 2 PHENOTYPE
A 0.700 CausalMutation CLINVAR
dbSNP: rs527843566
rs527843566
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C3889592
Disease:
BCHE, H VARIANT PHENOTYPE
T 0.700 CausalMutation CLINVAR
dbSNP: rs121918556
rs121918556
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C3889591
Disease:
BCHE, J VARIANT PHENOTYPE
A 0.700 CausalMutation CLINVAR
dbSNP: rs11447348
rs11447348
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C2985280
Disease:
Blood Protein Measurement
GA 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs1803274
rs1803274
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs2668196
rs2668196
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase. 2915989 1989
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT Naturally occurring mutation, Asp70his, in human butyrylcholinesterase. 11928765 2002
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT Four new mutations in the BCHE gene of human butyrylcholinesterase in a Brazilian blood donor sample. 15781196 2005
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity. 15563885 2005
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan. 9191541 1997
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT "Characterization of a novel butyrylcholinesterase point mutation (p.Ala34Val), ""silent"" with mivacurium." 25264279 2014
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT Characterization of an unstable variant (BChE115D) of human butyrylcholinesterase. 9110359 1997
dbSNP: rs104893684
rs104893684
Entrez Id: 590
Gene Symbol: BCHE
BCHE
CUI: C1283400
Disease:
Butyrylcholinesterase deficiency
0.800 GeneticVariation UNIPROT DNA mutations associated with the human butyrylcholinesterase J-variant. 1349196 1992