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rs397516052

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516052(-;-)
Make rs397516052(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position47350060
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516052
ebirs397516052
HLIrs397516052
Exacrs397516052
Varsomers397516052
Maprs397516052
PheGenIrs397516052
hapmaprs397516052
1000 genomesrs397516052
hgdprs397516052
ensemblrs397516052
gopubmedrs397516052
geneviewrs397516052
scholarrs397516052
googlers397516052
pharmgkbrs397516052
gwascentralrs397516052
openSNPrs397516052
23andMers397516052
23andMe allrs397516052
SNP Nexus

SNPshotrs397516052
SNPdbers397516052
MSV3drs397516052
GWAS Ctlgrs397516052
Max Magnitude0
ClinVar
Risk rs397516052(;)
Alt rs397516052(;)
Reference rs397516052(C;C)
Significance Other
Disease Familial hypertrophic cardiomyopathy 4 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47371611delG
CLNSRC ClinVar
CLNACC RCV000035630.4, RCV000158414.2, RCV000211828.1,