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rs730880610

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880610(C;T)
Make rs730880610(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350603
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880610
ebirs730880610
HLIrs730880610
Exacrs730880610
Varsomers730880610
Maprs730880610
PheGenIrs730880610
hapmaprs730880610
1000 genomesrs730880610
hgdprs730880610
ensemblrs730880610
gopubmedrs730880610
geneviewrs730880610
scholarrs730880610
googlers730880610
pharmgkbrs730880610
gwascentralrs730880610
openSNPrs730880610
23andMers730880610
23andMe allrs730880610
SNP Nexus

SNPshotrs730880610
SNPdbers730880610
MSV3drs730880610
GWAS Ctlgrs730880610
Max Magnitude0
ClinVar
Risk rs730880610(T;T)
Alt rs730880610(T;T)
Reference rs730880610(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47372154G>A
CLNSRC
CLNACC RCV000158274.2,