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rs730880620

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880620(A;A)
Make rs730880620(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350013
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880620
ebirs730880620
HLIrs730880620
Exacrs730880620
Varsomers730880620
Maprs730880620
PheGenIrs730880620
hapmaprs730880620
1000 genomesrs730880620
hgdprs730880620
ensemblrs730880620
gopubmedrs730880620
geneviewrs730880620
scholarrs730880620
googlers730880620
pharmgkbrs730880620
gwascentralrs730880620
openSNPrs730880620
23andMers730880620
23andMe allrs730880620
SNP Nexus

SNPshotrs730880620
SNPdbers730880620
MSV3drs730880620
GWAS Ctlgrs730880620
Max Magnitude0
ClinVar
Risk rs730880620(A;A)
Alt rs730880620(A;A)
Reference rs730880620(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47371564C>T
CLNSRC
CLNACC RCV000158288.2,