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rs730880577

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880577(C;T)
Make rs730880577(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335098
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880577
ebirs730880577
HLIrs730880577
Exacrs730880577
Varsomers730880577
Maprs730880577
PheGenIrs730880577
hapmaprs730880577
1000 genomesrs730880577
hgdprs730880577
ensemblrs730880577
gopubmedrs730880577
geneviewrs730880577
scholarrs730880577
googlers730880577
pharmgkbrs730880577
gwascentralrs730880577
openSNPrs730880577
23andMers730880577
23andMe allrs730880577
SNP Nexus

SNPshotrs730880577
SNPdbers730880577
MSV3drs730880577
GWAS Ctlgrs730880577
Max Magnitude0
ClinVar
Risk rs730880577(T;T)
Alt rs730880577(T;T)
Reference rs730880577(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47356649G>A
CLNSRC
CLNACC RCV000158190.2,