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rs730880641

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880641(G;G)
Make rs730880641(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343490
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880641
ebirs730880641
HLIrs730880641
Exacrs730880641
Varsomers730880641
Maprs730880641
PheGenIrs730880641
hapmaprs730880641
1000 genomesrs730880641
hgdprs730880641
ensemblrs730880641
gopubmedrs730880641
geneviewrs730880641
scholarrs730880641
googlers730880641
pharmgkbrs730880641
gwascentralrs730880641
openSNPrs730880641
23andMers730880641
23andMe allrs730880641
SNP Nexus

SNPshotrs730880641
SNPdbers730880641
MSV3drs730880641
GWAS Ctlgrs730880641
Max Magnitude0
ClinVar
Risk rs730880641(G;G)
Alt rs730880641(G;G)
Reference rs730880641(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47365041A>C
CLNSRC
CLNACC RCV000158342.1,