Have questions? Visit https://www.reddit.com/r/SNPedia

rs71534280

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs71534280(A;A)
Make rs71534280(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position68201918
GeneMYPN
is asnp
is mentioned by
dbSNPrs71534280
ebirs71534280
HLIrs71534280
Exacrs71534280
Varsomers71534280
Maprs71534280
PheGenIrs71534280
hapmaprs71534280
1000 genomesrs71534280
hgdprs71534280
ensemblrs71534280
gopubmedrs71534280
geneviewrs71534280
scholarrs71534280
googlers71534280
pharmgkbrs71534280
gwascentralrs71534280
openSNPrs71534280
23andMers71534280
23andMe allrs71534280
SNP Nexus

SNPshotrs71534280
SNPdbers71534280
MSV3drs71534280
GWAS Ctlgrs71534280
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs71534280(A;A)
Alt rs71534280(A;A)
Reference rs71534280(G;G)
Significance Pathogenic
Disease not provided Dilated cardiomyopathy 1KK not specified
Variation info
Gene MYPN
CLNDBN not provided Dilated cardiomyopathy 1KK not specified
Reversed 0
HGVS NC_000010.10:g.69961675G>A
CLNSRC Leiden Muscular Dystrophy pages (MYPN) OMIM Allelic Variant
CLNACC RCV000024485.2, RCV000043543.2, RCV000219549.1,


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