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rs730880557

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880557(A;C)
Make rs730880557(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341134
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880557
ebirs730880557
HLIrs730880557
Exacrs730880557
Varsomers730880557
Maprs730880557
PheGenIrs730880557
hapmaprs730880557
1000 genomesrs730880557
hgdprs730880557
ensemblrs730880557
gopubmedrs730880557
geneviewrs730880557
scholarrs730880557
googlers730880557
pharmgkbrs730880557
gwascentralrs730880557
openSNPrs730880557
23andMers730880557
23andMe allrs730880557
SNP Nexus

SNPshotrs730880557
SNPdbers730880557
MSV3drs730880557
GWAS Ctlgrs730880557
Max Magnitude0
ClinVar
Risk rs730880557(C;C)
Alt rs730880557(C;C)
Reference rs730880557(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47362685T>G
CLNSRC
CLNACC RCV000158129.1,