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rs397516014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516014(-;-)
Make rs397516014(-;G)
Make rs397516014(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47333226
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516014
ebirs397516014
HLIrs397516014
Exacrs397516014
Varsomers397516014
Maprs397516014
PheGenIrs397516014
hapmaprs397516014
1000 genomesrs397516014
hgdprs397516014
ensemblrs397516014
gopubmedrs397516014
geneviewrs397516014
scholarrs397516014
googlers397516014
pharmgkbrs397516014
gwascentralrs397516014
openSNPrs397516014
23andMers397516014
23andMe allrs397516014
SNP Nexus

SNPshotrs397516014
SNPdbers397516014
MSV3drs397516014
GWAS Ctlgrs397516014
Max Magnitude0
ClinVar
Risk rs397516014(G;G)
Alt rs397516014(G;G)
Reference rs397516014(;)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.47354778dupC
CLNSRC ClinVar
CLNACC RCV000157318.2, RCV000223806.1,