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rs730880665

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs730880665(-;-)
Make rs730880665(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333717
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880665
ebirs730880665
HLIrs730880665
Exacrs730880665
Varsomers730880665
Maprs730880665
PheGenIrs730880665
hapmaprs730880665
1000 genomesrs730880665
hgdprs730880665
ensemblrs730880665
gopubmedrs730880665
geneviewrs730880665
scholarrs730880665
googlers730880665
pharmgkbrs730880665
gwascentralrs730880665
openSNPrs730880665
23andMers730880665
23andMe allrs730880665
SNP Nexus

SNPshotrs730880665
SNPdbers730880665
MSV3drs730880665
GWAS Ctlgrs730880665
Max Magnitude0
ClinVar
Risk rs730880665(;)
Alt rs730880665(;)
Reference rs730880665(AG;AG)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355268_47355269delCT
CLNSRC
CLNACC RCV000158388.1,