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rs730880536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880536(A;A)
Make rs730880536(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342932
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880536
ClinGenrs730880536
ebirs730880536
HLIrs730880536
Exacrs730880536
Varsomers730880536
Maprs730880536
PheGenIrs730880536
hapmaprs730880536
1000 genomesrs730880536
hgdprs730880536
ensemblrs730880536
gopubmedrs730880536
geneviewrs730880536
scholarrs730880536
googlers730880536
pharmgkbrs730880536
gwascentralrs730880536
openSNPrs730880536
23andMers730880536
23andMe allrs730880536
SNP Nexus

SNPshotrs730880536
SNPdbers730880536
MSV3drs730880536
GWAS Ctlgrs730880536
Max Magnitude0
ClinVar
Risk rs730880536(A;A)
Alt rs730880536(A;A)
Reference Rs730880536(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364483G>T
CLNSRC
CLNACC RCV000158077.2,