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rs71584501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs71584501(A;A)
Make rs71584501(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position68197456
GeneMYPN
is asnp
is mentioned by
dbSNPrs71584501
ebirs71584501
HLIrs71584501
Exacrs71584501
Varsomers71584501
Maprs71584501
PheGenIrs71584501
hapmaprs71584501
1000 genomesrs71584501
hgdprs71584501
ensemblrs71584501
gopubmedrs71584501
geneviewrs71584501
scholarrs71584501
googlers71584501
pharmgkbrs71584501
gwascentralrs71584501
openSNPrs71584501
23andMers71584501
23andMe allrs71584501
SNP Nexus

SNPshotrs71584501
SNPdbers71584501
MSV3drs71584501
GWAS Ctlgrs71584501
Max Magnitude0
ClinVar
Risk rs71584501(A;A)
Alt rs71584501(A;A)
Reference rs71584501(G;G)
Significance Pathogenic
Disease not provided Dilated cardiomyopathy 1KK
Variation info
Gene MYPN
CLNDBN not provided Dilated cardiomyopathy 1KK
Reversed 0
HGVS NC_000010.10:g.69957213G>A
CLNSRC Leiden Muscular Dystrophy pages (MYPN) OMIM Allelic Variant
CLNACC RCV000024483.1, RCV000043540.2,


[PMID 18006477] Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy.