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rs730880539

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880539(C;T)
Make rs730880539(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342882
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880539
ebirs730880539
HLIrs730880539
Exacrs730880539
Varsomers730880539
Maprs730880539
PheGenIrs730880539
hapmaprs730880539
1000 genomesrs730880539
hgdprs730880539
ensemblrs730880539
gopubmedrs730880539
geneviewrs730880539
scholarrs730880539
googlers730880539
pharmgkbrs730880539
gwascentralrs730880539
openSNPrs730880539
23andMers730880539
23andMe allrs730880539
SNP Nexus

SNPshotrs730880539
SNPdbers730880539
MSV3drs730880539
GWAS Ctlgrs730880539
Max Magnitude0
ClinVar
Risk rs730880539(G,T;G,T)
Alt rs730880539(G,T;G,T)
Reference rs730880539(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364433G>A
CLNSRC
CLNACC RCV000158082.1,