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rs397516050

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516050(A;A)
Make rs397516050(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350077
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516050
ebirs397516050
HLIrs397516050
Exacrs397516050
Varsomers397516050
Maprs397516050
PheGenIrs397516050
hapmaprs397516050
1000 genomesrs397516050
hgdprs397516050
ensemblrs397516050
gopubmedrs397516050
geneviewrs397516050
scholarrs397516050
googlers397516050
pharmgkbrs397516050
gwascentralrs397516050
openSNPrs397516050
23andMers397516050
23andMe allrs397516050
SNP Nexus

SNPshotrs397516050
SNPdbers397516050
MSV3drs397516050
GWAS Ctlgrs397516050
Max Magnitude0
ClinVar
Risk rs397516050(A;A)
Alt rs397516050(A;A)
Reference rs397516050(G;G)
Significance Pathogenic
Disease not specified not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47371628C>T
CLNSRC
CLNACC RCV000035627.4, RCV000172015.1, RCV000206268.2,