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rs730880637

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880637(C;T)
Make rs730880637(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343514
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880637
ebirs730880637
HLIrs730880637
Exacrs730880637
Varsomers730880637
Maprs730880637
PheGenIrs730880637
hapmaprs730880637
1000 genomesrs730880637
hgdprs730880637
ensemblrs730880637
gopubmedrs730880637
geneviewrs730880637
scholarrs730880637
googlers730880637
pharmgkbrs730880637
gwascentralrs730880637
openSNPrs730880637
23andMers730880637
23andMe allrs730880637
SNP Nexus

SNPshotrs730880637
SNPdbers730880637
MSV3drs730880637
GWAS Ctlgrs730880637
Max Magnitude0
ClinVar
Risk rs730880637(T;T)
Alt rs730880637(T;T)
Reference rs730880637(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47365065G>A
CLNSRC
CLNACC RCV000158336.1,