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rs730880573

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880573(C;T)
Make rs730880573(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351485
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880573
ebirs730880573
HLIrs730880573
Exacrs730880573
Varsomers730880573
Maprs730880573
PheGenIrs730880573
hapmaprs730880573
1000 genomesrs730880573
hgdprs730880573
ensemblrs730880573
gopubmedrs730880573
geneviewrs730880573
scholarrs730880573
googlers730880573
pharmgkbrs730880573
gwascentralrs730880573
openSNPrs730880573
23andMers730880573
23andMe allrs730880573
SNP Nexus

SNPshotrs730880573
SNPdbers730880573
MSV3drs730880573
GWAS Ctlgrs730880573
Max Magnitude0
ClinVar
Risk rs730880573(T;T)
Alt rs730880573(T;T)
Reference rs730880573(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47373036G>A
CLNSRC
CLNACC RCV000158175.2,