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rs140148105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs140148105(A;G)
Make rs140148105(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position68121497
GeneMYPN
is asnp
is mentioned by
dbSNPrs140148105
ebirs140148105
HLIrs140148105
Exacrs140148105
Varsomers140148105
Maprs140148105
PheGenIrs140148105
hapmaprs140148105
1000 genomesrs140148105
hgdprs140148105
ensemblrs140148105
gopubmedrs140148105
geneviewrs140148105
scholarrs140148105
googlers140148105
pharmgkbrs140148105
gwascentralrs140148105
openSNPrs140148105
23andMers140148105
23andMe allrs140148105
SNP Nexus

SNPshotrs140148105
SNPdbers140148105
MSV3drs140148105
GWAS Ctlgrs140148105
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs140148105(G;G)
Alt rs140148105(G;G)
Reference rs140148105(A;A)
Significance Other
Disease not provided Familial hypertrophic cardiomyopathy 22 Dilated cardiomyopathy 1KK Primary dilated cardiomyopathy not specified
Variation info
Gene MYPN
CLNDBN not provided Familial hypertrophic cardiomyopathy 22 Dilated cardiomyopathy 1KK Primary dilated cardiomyopathy not specified
Reversed 0
HGVS NC_000010.10:g.69881254A>G
CLNSRC Leiden Muscular Dystrophy pages (MYPN) OMIM Allelic Variant
CLNACC RCV000024504.2, RCV000043545.2, RCV000043546.3, RCV000157381.1, RCV000183576.3,


[PMID 22286171OA-icon.png] Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.