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rs730880598

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880598(G;T)
Make rs730880598(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332222
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880598
ebirs730880598
HLIrs730880598
Exacrs730880598
Varsomers730880598
Maprs730880598
PheGenIrs730880598
hapmaprs730880598
1000 genomesrs730880598
hgdprs730880598
ensemblrs730880598
gopubmedrs730880598
geneviewrs730880598
scholarrs730880598
googlers730880598
pharmgkbrs730880598
gwascentralrs730880598
openSNPrs730880598
23andMers730880598
23andMe allrs730880598
SNP Nexus

SNPshotrs730880598
SNPdbers730880598
MSV3drs730880598
GWAS Ctlgrs730880598
Max Magnitude0
ClinVar
Risk rs730880598(T;T)
Alt rs730880598(T;T)
Reference rs730880598(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47353773C>A
CLNSRC
CLNACC RCV000158250.1,