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rs730880603

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880603(A;A)
Make rs730880603(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332115
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880603
ebirs730880603
HLIrs730880603
Exacrs730880603
Varsomers730880603
Maprs730880603
PheGenIrs730880603
hapmaprs730880603
1000 genomesrs730880603
hgdprs730880603
ensemblrs730880603
gopubmedrs730880603
geneviewrs730880603
scholarrs730880603
googlers730880603
pharmgkbrs730880603
gwascentralrs730880603
openSNPrs730880603
23andMers730880603
23andMe allrs730880603
SNP Nexus

SNPshotrs730880603
SNPdbers730880603
MSV3drs730880603
GWAS Ctlgrs730880603
Max Magnitude0
ClinVar
Risk rs730880603(A;A)
Alt rs730880603(A;A)
Reference rs730880603(C;C)
Significance Probable-Pathogenic
Disease not provided not specified Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353666G>T
CLNSRC
CLNACC RCV000158261.2, RCV000215436.2, RCV000234005.1,