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rs730880708

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880708(C;C)
Make rs730880708(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346333
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880708
ebirs730880708
HLIrs730880708
Exacrs730880708
Varsomers730880708
Maprs730880708
PheGenIrs730880708
hapmaprs730880708
1000 genomesrs730880708
hgdprs730880708
ensemblrs730880708
gopubmedrs730880708
geneviewrs730880708
scholarrs730880708
googlers730880708
pharmgkbrs730880708
gwascentralrs730880708
openSNPrs730880708
23andMers730880708
23andMe allrs730880708
SNP Nexus

SNPshotrs730880708
SNPdbers730880708
MSV3drs730880708
GWAS Ctlgrs730880708
Max Magnitude0
ClinVar
Risk rs730880708(C;C)
Alt rs730880708(C;C)
Reference rs730880708(T;T)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYBPC3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000011.9:g.47367884A>G
CLNSRC
CLNACC RCV000158470.1, RCV000223765.1,