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rs730880587

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880587(A;A)
Make rs730880587(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333661
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880587
ebirs730880587
HLIrs730880587
Exacrs730880587
Varsomers730880587
Maprs730880587
PheGenIrs730880587
hapmaprs730880587
1000 genomesrs730880587
hgdprs730880587
ensemblrs730880587
gopubmedrs730880587
geneviewrs730880587
scholarrs730880587
googlers730880587
pharmgkbrs730880587
gwascentralrs730880587
openSNPrs730880587
23andMers730880587
23andMe allrs730880587
SNP Nexus

SNPshotrs730880587
SNPdbers730880587
MSV3drs730880587
GWAS Ctlgrs730880587
Max Magnitude0
ClinVar
Risk rs730880587(A;A)
Alt rs730880587(A;A)
Reference rs730880587(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47355212A>T
CLNSRC
CLNACC RCV000158213.1,