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rs376395543

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs376395543(C;C)
Make rs376395543(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47351507
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs376395543
ebirs376395543
HLIrs376395543
Exacrs376395543
Varsomers376395543
Maprs376395543
PheGenIrs376395543
hapmaprs376395543
1000 genomesrs376395543
hgdprs376395543
ensemblrs376395543
gopubmedrs376395543
geneviewrs376395543
scholarrs376395543
googlers376395543
pharmgkbrs376395543
gwascentralrs376395543
openSNPrs376395543
23andMers376395543
23andMe allrs376395543
SNP Nexus

SNPshotrs376395543
SNPdbers376395543
MSV3drs376395543
GWAS Ctlgrs376395543
Max Magnitude0
ClinVar
Risk rs376395543(C;C)
Alt rs376395543(C;C)
Reference rs376395543(T;T)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 0
HGVS NC_000011.9:g.47373058T>C
CLNSRC ClinVar
CLNACC RCV000035512.4, RCV000158174.2,