CHRM3, cholinergic receptor muscarinic 3, 1131

N. diseases: 284; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12059546
rs12059546
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0014544
Disease:
Epilepsy
G 0.800 GeneticVariation GWASCAT Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. 22949513 2012
dbSNP: rs12059546
rs12059546
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0014544
Disease:
Epilepsy
G 0.800 GeneticVariation GWASDB Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. 22949513 2012
dbSNP: rs11579382
rs11579382
Entrez Id: 1131;100506915
Gene Symbol: CHRM3;CHRM3-AS2
CHRM3;CHRM3-AS2
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
C 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs12036147
rs12036147
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C1269683
Disease:
Major Depressive Disorder
A 0.700 GeneticVariation GWASCAT GWAS and systems biology analysis of depressive symptoms among smokers from the COPDGene cohort. 30219690 2019
dbSNP: rs12036147
rs12036147
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0037369
Disease:
Smoking
A 0.700 GeneticVariation GWASCAT GWAS and systems biology analysis of depressive symptoms among smokers from the COPDGene cohort. 30219690 2019
dbSNP: rs2355237
rs2355237
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C1518922
Disease:
peak expiratory flow (procedure)
A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs2355237
rs2355237
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0016529
Disease:
Forced expiratory volume function
A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs12082628
rs12082628
Entrez Id: 1131;105373225
Gene Symbol: CHRM3;LOC105373225
CHRM3;LOC105373225
CUI: C0272178
Disease:
Drug-induced neutropenia
0.700 GeneticVariation GWASCAT Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus. 28762467 2018
dbSNP: rs16838623
rs16838623
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C3897558
Disease:
Soluble Interleukin 6 Receptor Measurement
0.700 GeneticVariation GWASCAT Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. 28820441 2017
dbSNP: rs16838623
rs16838623
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C1281901
Disease:
Fatty acid measurement
0.700 GeneticVariation GWASCAT Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. 28820441 2017
dbSNP: rs185275068
rs185275068
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0016529
Disease:
Forced expiratory volume function
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs188686089
rs188686089
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0016529
Disease:
Forced expiratory volume function
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs76759221
rs76759221
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0016529
Disease:
Forced expiratory volume function
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs77830002
rs77830002
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0016529
Disease:
Forced expiratory volume function
T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs536477
rs536477
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C1861172
Disease:
Venous Thromboembolism
0.700 GeneticVariation GWASDB A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. 23509962 2013
dbSNP: rs587776862
rs587776862
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0033770
Disease:
Prune Belly Syndrome
T 0.700 CausalMutation CLINVAR
dbSNP: rs2165870
rs2165870
Entrez Id: 1131;105373225
Gene Symbol: CHRM3;LOC105373225
CHRM3;LOC105373225
CUI: C0520909
Disease:
Postoperative Nausea and Vomiting
0.020 GeneticVariation BEFREE The KCNB2 SNP was associated with an Odds Ratio (OR) of 1.6 for CT/CC vs. TT (95% CI 1-2.5; P = 0.031) to develop PONV and this was independent from the Apfel Score, and the CHRM3 rs2165870 SNP. 31077873 2020
dbSNP: rs2165870
rs2165870
Entrez Id: 1131;105373225
Gene Symbol: CHRM3;LOC105373225
CHRM3;LOC105373225
CUI: C0520909
Disease:
Postoperative Nausea and Vomiting
0.020 GeneticVariation BEFREE Early PONV occurred in 37% of subjects.The rs2165870 genotype distribution was GG in 191, GA in 207, and AA in 56 subjects. 29935595 2018
dbSNP: rs4620530
rs4620530
Entrez Id: 1131;100873984
Gene Symbol: CHRM3;CHRM3-AS1
CHRM3;CHRM3-AS1
CUI: C0008312
Disease:
Primary biliary cirrhosis
0.010 GeneticVariation BEFREE CHRM3 single-nucleotide polymorphism rs4620530 might confer an increased genetic risk for the development of PBC. 31747477 2020
dbSNP: rs4620530
rs4620530
Entrez Id: 1131;100873984
Gene Symbol: CHRM3;CHRM3-AS1
CHRM3;CHRM3-AS1
CUI: C0566602
Disease:
Primary sclerosing cholangitis
0.010 GeneticVariation BEFREE CHRM3 rs4620530 proportions in patients with PBC significantly differed from patients with PSC (P = 0.005), CHC (P = 0.009), and healthy controls (P = 0.008), primarily due to a substantial overrepresentation of the T allele in PBC (49.3% in PBC vs. 39.8% in PSC, 35.7% in CHC, and 40% in healthy controls), indicating a potential association of the rs4620530 T allele with PBC (OR 1.461, 95% CI 1.147-1.861, P = 0.002). 31747477 2020
dbSNP: rs1867265
rs1867265
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0032460
Disease:
Polycystic Ovary Syndrome
0.010 GeneticVariation BEFREE The 6 genetic variants involved in brain and nervous system (acid sensing ion channel subunit 2 rs8071961, rs1988598, and rs16589, macro domain containing 2 rs7262810 CHRM3 rs1867265 and chromosome 2 open reading frame 83 rs11889798) were selected from a GWAS of the PCOS study. 30343302 2019
dbSNP: rs12059546
rs12059546
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0270853
Disease:
Juvenile Myoclonic Epilepsy
0.010 GeneticVariation BEFREE The search for syndrome-related susceptibility alleles identified significant associations for GAEs at 2q22.3 (rs10496964, P(meta) = 9.1 × 10(-9), OR[T] = 0.68) and at 1q43 for JME (rs12059546, P(meta) = 4.1 × 10(-8), OR[G] = 1.42). 22949513 2012
dbSNP: rs3738435
rs3738435
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0020456
Disease:
Hyperglycemia
0.010 GeneticVariation BEFREE There was no association of CHRM3 gene variant rs3738435 with BMI, and we observed no association with HbA1c or hyperglycaemia in any of the variants. 21336576 2011
dbSNP: rs3738435
rs3738435
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE To better assess whether this variant has a role in acute insulin secretion, which could affect risk for early-onset type 2 diabetes, rs3738435 was genotyped in a larger group of normal glucose-tolerant Pima Indians who had measures of acute insulin secretion (n = 282) and a larger case-control group of Pima Indians selected for early-onset type 2 diabetes (n = 348 case subjects with age of onset <25 years; n = 392 nondiabetic control subjects aged >45 years). 17130513 2006
dbSNP: rs771480057
rs771480057
Entrez Id: 1131
Gene Symbol: CHRM3
CHRM3
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
0.010 GeneticVariation BEFREE In mice that express the mutant human gene Cu/Zn superoxide dismutase G93A (SOD1), and therefore simulate the chronic human motor neuron disease amyotrophic lateral sclerosis, Cop-1 vaccination prolonged life span compared to untreated matched controls, from 211 +/- 7 days (n = 15) to 263 +/- 8 days (n = 14; P < 0.0001). 12668759 2003