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

rs397515885

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515885(A;A)
Make rs397515885(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351427
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515885
ebirs397515885
HLIrs397515885
Exacrs397515885
Varsomers397515885
Maprs397515885
PheGenIrs397515885
hapmaprs397515885
1000 genomesrs397515885
hgdprs397515885
ensemblrs397515885
gopubmedrs397515885
geneviewrs397515885
scholarrs397515885
googlers397515885
pharmgkbrs397515885
gwascentralrs397515885
openSNPrs397515885
23andMers397515885
23andMe allrs397515885
SNP Nexus

SNPshotrs397515885
SNPdbers397515885
MSV3drs397515885
GWAS Ctlgrs397515885
Max Magnitude0
ClinVar
Risk rs397515885(A;A)
Alt rs397515885(A;A)
Reference rs397515885(G;G)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47372978C>T
CLNSRC
CLNACC RCV000035368.2, RCV000158185.1,