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rs730880531

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880531(A;G)
Make rs730880531(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343147
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880531
ebirs730880531
HLIrs730880531
Exacrs730880531
Varsomers730880531
Maprs730880531
PheGenIrs730880531
hapmaprs730880531
1000 genomesrs730880531
hgdprs730880531
ensemblrs730880531
gopubmedrs730880531
geneviewrs730880531
scholarrs730880531
googlers730880531
pharmgkbrs730880531
gwascentralrs730880531
openSNPrs730880531
23andMers730880531
23andMe allrs730880531
SNP Nexus

SNPshotrs730880531
SNPdbers730880531
MSV3drs730880531
GWAS Ctlgrs730880531
Max Magnitude0
ClinVar
Risk rs730880531(G;G)
Alt rs730880531(G;G)
Reference rs730880531(A;A)
Significance Other
Disease not provided Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN not provided Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47364698T>C
CLNSRC
CLNACC RCV000158068.2, RCV000168772.1,