MYOCD, myocardin, 93649

N. diseases: 79; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35712872
rs35712872
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		G 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. 30679814 2019
dbSNP: rs1984481
rs1984481
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		C 0.700 GeneticVariation GWASCAT PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. 30046033 2018
dbSNP: rs72811294
rs72811294
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C0004238
Disease:
Atrial Fibrillation 		G 0.700 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015 2018
dbSNP: rs72811294
rs72811294
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C0004238
Disease:
Atrial Fibrillation 		G 0.700 GeneticVariation GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
dbSNP: rs9913758
rs9913758
Entrez Id: 93649;100128006
Gene Symbol: MYOCD;LOC100128006
MYOCD;LOC100128006
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs9913758
rs9913758
Entrez Id: 93649;100128006
Gene Symbol: MYOCD;LOC100128006
MYOCD;LOC100128006
CUI: C0428474
Disease:
Serum LDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs9913758
rs9913758
Entrez Id: 93649;100128006
Gene Symbol: MYOCD;LOC100128006
MYOCD;LOC100128006
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs9913758
rs9913758
Entrez Id: 93649;100128006
Gene Symbol: MYOCD;LOC100128006
MYOCD;LOC100128006
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs137939966
rs137939966
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C0036572
Disease:
Seizures 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs137939966
rs137939966
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C1843367
Disease:
Poor school performance 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1714984
rs1714984
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C0019337
Disease:
Heroin Dependence 		0.010 GeneticVariation BEFREE The three variants exhibiting the strongest association with heroin addiction by genotype frequency were rs1714984, located in an intron of the gene for the transcription factor myocardin (P=0.000022), rs965972 (P=0.000080) and rs1867898 (P=0.000284). 18195715 2008
dbSNP: rs760414580
rs760414580
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
CUI: C0152021
Disease:
Congenital heart disease 		0.010 GeneticVariation BEFREE We identified a rare human sequence variation in MYOCD in a patient with congenital heart disease that resulted in a missense mutation at codon 259 (K259R). 18852265 2008