MIR208A, microRNA 208a, 406990

N. diseases: 38; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs150815925
rs150815925
Entrez Id: 4624;406990
Gene Symbol: MYH6;MIR208A
MYH6;MIR208A
CUI: C0010068
Disease:
Coronary heart disease 		0.010 GeneticVariation BEFREE Fourteen variants were present in public databases with very rare allele frequency, of which four variants (p.Arg25Cys in NKX2-5, p.Val763Ile in ZFPM2, p.Arg1398Gln and Gly1826Asp in MYH6) have been previously linked to CHD or cardiomyopathy. 29332214 2018
dbSNP: rs150815925
rs150815925
Entrez Id: 4624;406990
Gene Symbol: MYH6;MIR208A
MYH6;MIR208A
CUI: C0878544
Disease:
Cardiomyopathies 		0.010 GeneticVariation BEFREE Fourteen variants were present in public databases with very rare allele frequency, of which four variants (p.Arg25Cys in NKX2-5, p.Val763Ile in ZFPM2, p.Arg1398Gln and Gly1826Asp in MYH6) have been previously linked to CHD or cardiomyopathy. 29332214 2018
dbSNP: rs751426149
rs751426149
Entrez Id: 4624;406990
Gene Symbol: MYH6;MIR208A
MYH6;MIR208A
CUI: C0152021
Disease:
Congenital heart disease 		0.010 GeneticVariation BEFREE Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease. 29969989 2018