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rs397516076

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516076(C;C)
Make rs397516076(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47347855
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516076
ClinGenrs397516076
ebirs397516076
HLIrs397516076
Exacrs397516076
Varsomers397516076
Maprs397516076
PheGenIrs397516076
hapmaprs397516076
1000 genomesrs397516076
hgdprs397516076
ensemblrs397516076
gopubmedrs397516076
geneviewrs397516076
scholarrs397516076
googlers397516076
pharmgkbrs397516076
gwascentralrs397516076
openSNPrs397516076
23andMers397516076
23andMe allrs397516076
SNP Nexus

SNPshotrs397516076
SNPdbers397516076
MSV3drs397516076
GWAS Ctlgrs397516076
Max Magnitude0
ClinVar
Risk rs397516076(C;C)
Alt rs397516076(C;C)
Reference Rs397516076(T;T)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 1
HGVS NC_000011.9:g.47369406A>G
CLNSRC ClinVar
CLNACC RCV000035671.3, RCV000168758.1,