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rs730880586

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880586(C;T)
Make rs730880586(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333713
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880586
ebirs730880586
HLIrs730880586
Exacrs730880586
Varsomers730880586
Maprs730880586
PheGenIrs730880586
hapmaprs730880586
1000 genomesrs730880586
hgdprs730880586
ensemblrs730880586
gopubmedrs730880586
geneviewrs730880586
scholarrs730880586
googlers730880586
pharmgkbrs730880586
gwascentralrs730880586
openSNPrs730880586
23andMers730880586
23andMe allrs730880586
SNP Nexus

SNPshotrs730880586
SNPdbers730880586
MSV3drs730880586
GWAS Ctlgrs730880586
Max Magnitude0
ClinVar
Risk rs730880586(T;T)
Alt rs730880586(T;T)
Reference rs730880586(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47355264G>A
CLNSRC
CLNACC RCV000158209.2,