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rs730880699

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880699(C;T)
Make rs730880699(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332640
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880699
ebirs730880699
HLIrs730880699
Exacrs730880699
Varsomers730880699
Maprs730880699
PheGenIrs730880699
hapmaprs730880699
1000 genomesrs730880699
hgdprs730880699
ensemblrs730880699
gopubmedrs730880699
geneviewrs730880699
scholarrs730880699
googlers730880699
pharmgkbrs730880699
gwascentralrs730880699
openSNPrs730880699
23andMers730880699
23andMe allrs730880699
SNP Nexus

SNPshotrs730880699
SNPdbers730880699
MSV3drs730880699
GWAS Ctlgrs730880699
Max Magnitude0
ClinVar
Risk rs730880699(T;T)
Alt rs730880699(T;T)
Reference rs730880699(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47354191G>A
CLNSRC
CLNACC RCV000158453.2,