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rs397515966

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515966(-;-)
Make rs397515966(-;T)
Make rs397515966(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47337502
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515966
ebirs397515966
HLIrs397515966
Exacrs397515966
Varsomers397515966
Maprs397515966
PheGenIrs397515966
hapmaprs397515966
1000 genomesrs397515966
hgdprs397515966
ensemblrs397515966
gopubmedrs397515966
geneviewrs397515966
scholarrs397515966
googlers397515966
pharmgkbrs397515966
gwascentralrs397515966
openSNPrs397515966
23andMers397515966
23andMe allrs397515966
SNP Nexus

SNPshotrs397515966
SNPdbers397515966
MSV3drs397515966
GWAS Ctlgrs397515966
Max Magnitude0
ClinVar
Risk rs397515966(T;T)
Alt rs397515966(T;T)
Reference rs397515966(;)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy Cardiomyopathy Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy Cardiomyopathy Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47359054dupA
CLNSRC ClinVar
CLNACC RCV000157328.3, RCV000158365.1, RCV000232323.1,