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rs730880576

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880576(A;A)
Make rs730880576(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335199
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880576
ebirs730880576
HLIrs730880576
Exacrs730880576
Varsomers730880576
Maprs730880576
PheGenIrs730880576
hapmaprs730880576
1000 genomesrs730880576
hgdprs730880576
ensemblrs730880576
gopubmedrs730880576
geneviewrs730880576
scholarrs730880576
googlers730880576
pharmgkbrs730880576
gwascentralrs730880576
openSNPrs730880576
23andMers730880576
23andMe allrs730880576
SNP Nexus

SNPshotrs730880576
SNPdbers730880576
MSV3drs730880576
GWAS Ctlgrs730880576
Max Magnitude0
ClinVar
Risk rs730880576(A;A)
Alt rs730880576(A;A)
Reference rs730880576(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47356750C>T
CLNSRC
CLNACC RCV000158186.1,