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rs730880549

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880549(A;A)
Make rs730880549(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47342111
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880549
ebirs730880549
HLIrs730880549
Exacrs730880549
Varsomers730880549
Maprs730880549
PheGenIrs730880549
hapmaprs730880549
1000 genomesrs730880549
hgdprs730880549
ensemblrs730880549
gopubmedrs730880549
geneviewrs730880549
scholarrs730880549
googlers730880549
pharmgkbrs730880549
gwascentralrs730880549
openSNPrs730880549
23andMers730880549
23andMe allrs730880549
SNP Nexus

SNPshotrs730880549
SNPdbers730880549
MSV3drs730880549
GWAS Ctlgrs730880549
Max Magnitude0
ClinVar
Risk rs730880549(A;A)
Alt rs730880549(A;A)
Reference rs730880549(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYBPC3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000011.9:g.47363662C>T
CLNSRC
CLNACC RCV000158108.2, RCV000220868.1,