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rs730880567

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880567(A;A)
Make rs730880567(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337466
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880567
ebirs730880567
HLIrs730880567
Exacrs730880567
Varsomers730880567
Maprs730880567
PheGenIrs730880567
hapmaprs730880567
1000 genomesrs730880567
hgdprs730880567
ensemblrs730880567
gopubmedrs730880567
geneviewrs730880567
scholarrs730880567
googlers730880567
pharmgkbrs730880567
gwascentralrs730880567
openSNPrs730880567
23andMers730880567
23andMe allrs730880567
SNP Nexus

SNPshotrs730880567
SNPdbers730880567
MSV3drs730880567
GWAS Ctlgrs730880567
Max Magnitude0
ClinVar
Risk rs730880567(A;A)
Alt rs730880567(A;A)
Reference rs730880567(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47359017C>T
CLNSRC
CLNACC RCV000158164.2,