Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516024

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516024(G;G)
Make rs397516024(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47332645
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516024
ebirs397516024
HLIrs397516024
Exacrs397516024
Varsomers397516024
Maprs397516024
PheGenIrs397516024
hapmaprs397516024
1000 genomesrs397516024
hgdprs397516024
ensemblrs397516024
gopubmedrs397516024
geneviewrs397516024
scholarrs397516024
googlers397516024
pharmgkbrs397516024
gwascentralrs397516024
openSNPrs397516024
23andMers397516024
23andMe allrs397516024
SNP Nexus

SNPshotrs397516024
SNPdbers397516024
MSV3drs397516024
GWAS Ctlgrs397516024
Max Magnitude0
ClinVar
Risk rs397516024(G;G)
Alt rs397516024(G;G)
Reference rs397516024(T;T)
Significance Probable-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.47354196A>C
CLNSRC ClinVar
CLNACC RCV000035595.2, RCV000168820.1,