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rs730880608

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880608(C;C)
Make rs730880608(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332090
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880608
ebirs730880608
HLIrs730880608
Exacrs730880608
Varsomers730880608
Maprs730880608
PheGenIrs730880608
hapmaprs730880608
1000 genomesrs730880608
hgdprs730880608
ensemblrs730880608
gopubmedrs730880608
geneviewrs730880608
scholarrs730880608
googlers730880608
pharmgkbrs730880608
gwascentralrs730880608
openSNPrs730880608
23andMers730880608
23andMe allrs730880608
SNP Nexus

SNPshotrs730880608
SNPdbers730880608
MSV3drs730880608
GWAS Ctlgrs730880608
Max Magnitude0
ClinVar
Risk rs730880608(C;C)
Alt rs730880608(C;C)
Reference rs730880608(T;T)
Significance Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47353641A>G
CLNSRC
CLNACC RCV000158269.2,