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rs730880582

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880582(A;C)
Make rs730880582(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333974
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880582
ebirs730880582
HLIrs730880582
Exacrs730880582
Varsomers730880582
Maprs730880582
PheGenIrs730880582
hapmaprs730880582
1000 genomesrs730880582
hgdprs730880582
ensemblrs730880582
gopubmedrs730880582
geneviewrs730880582
scholarrs730880582
googlers730880582
pharmgkbrs730880582
gwascentralrs730880582
openSNPrs730880582
23andMers730880582
23andMe allrs730880582
SNP Nexus

SNPshotrs730880582
SNPdbers730880582
MSV3drs730880582
GWAS Ctlgrs730880582
Max Magnitude0
ClinVar
Risk rs730880582(C;C)
Alt rs730880582(C;C)
Reference rs730880582(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYBPC3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000011.9:g.47355525T>G
CLNSRC
CLNACC RCV000158201.1, RCV000223801.1,