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rs730880551

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880551(C;T)
Make rs730880551(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341230
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880551
ebirs730880551
HLIrs730880551
Exacrs730880551
Varsomers730880551
Maprs730880551
PheGenIrs730880551
hapmaprs730880551
1000 genomesrs730880551
hgdprs730880551
ensemblrs730880551
gopubmedrs730880551
geneviewrs730880551
scholarrs730880551
googlers730880551
pharmgkbrs730880551
gwascentralrs730880551
openSNPrs730880551
23andMers730880551
23andMe allrs730880551
SNP Nexus

SNPshotrs730880551
SNPdbers730880551
MSV3drs730880551
GWAS Ctlgrs730880551
Max Magnitude0
ClinVar
Risk rs730880551(T;T)
Alt rs730880551(T;T)
Reference rs730880551(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47362781G>A
CLNSRC
CLNACC RCV000158117.2,