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rs730880535

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880535(A;A)
Make rs730880535(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343063
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880535
ebirs730880535
HLIrs730880535
Exacrs730880535
Varsomers730880535
Maprs730880535
PheGenIrs730880535
hapmaprs730880535
1000 genomesrs730880535
hgdprs730880535
ensemblrs730880535
gopubmedrs730880535
geneviewrs730880535
scholarrs730880535
googlers730880535
pharmgkbrs730880535
gwascentralrs730880535
openSNPrs730880535
23andMers730880535
23andMe allrs730880535
SNP Nexus

SNPshotrs730880535
SNPdbers730880535
MSV3drs730880535
GWAS Ctlgrs730880535
Max Magnitude0
ClinVar
Risk rs730880535(A,T;A,T)
Alt rs730880535(A,T;A,T)
Reference rs730880535(G;G)
Significance Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364614C>T
CLNSRC
CLNACC RCV000158075.2, RCV000226142.1,