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rs730880552

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880552(C;T)
Make rs730880552(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341213
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880552
ebirs730880552
HLIrs730880552
Exacrs730880552
Varsomers730880552
Maprs730880552
PheGenIrs730880552
hapmaprs730880552
1000 genomesrs730880552
hgdprs730880552
ensemblrs730880552
gopubmedrs730880552
geneviewrs730880552
scholarrs730880552
googlers730880552
pharmgkbrs730880552
gwascentralrs730880552
openSNPrs730880552
23andMers730880552
23andMe allrs730880552
SNP Nexus

SNPshotrs730880552
SNPdbers730880552
MSV3drs730880552
GWAS Ctlgrs730880552
Max Magnitude0
ClinVar
Risk rs730880552(T;T)
Alt rs730880552(T;T)
Reference rs730880552(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47362764G>A
CLNSRC
CLNACC RCV000158121.2,