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rs730880570

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880570(A;T)
Make rs730880570(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337444
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880570
ebirs730880570
HLIrs730880570
Exacrs730880570
Varsomers730880570
Maprs730880570
PheGenIrs730880570
hapmaprs730880570
1000 genomesrs730880570
hgdprs730880570
ensemblrs730880570
gopubmedrs730880570
geneviewrs730880570
scholarrs730880570
googlers730880570
pharmgkbrs730880570
gwascentralrs730880570
openSNPrs730880570
23andMers730880570
23andMe allrs730880570
SNP Nexus

SNPshotrs730880570
SNPdbers730880570
MSV3drs730880570
GWAS Ctlgrs730880570
Max Magnitude0
ClinVar
Risk rs730880570(T;T)
Alt rs730880570(T;T)
Reference rs730880570(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47358995T>A
CLNSRC
CLNACC RCV000158170.2,