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rs730880538

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880538(C;T)
Make rs730880538(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342900
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880538
ebirs730880538
HLIrs730880538
Exacrs730880538
Varsomers730880538
Maprs730880538
PheGenIrs730880538
hapmaprs730880538
1000 genomesrs730880538
hgdprs730880538
ensemblrs730880538
gopubmedrs730880538
geneviewrs730880538
scholarrs730880538
googlers730880538
pharmgkbrs730880538
gwascentralrs730880538
openSNPrs730880538
23andMers730880538
23andMe allrs730880538
SNP Nexus

SNPshotrs730880538
SNPdbers730880538
MSV3drs730880538
GWAS Ctlgrs730880538
Max Magnitude0
ClinVar
Risk rs730880538(T;T)
Alt rs730880538(T;T)
Reference rs730880538(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364451G>A
CLNSRC
CLNACC RCV000158080.1,