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rs730880677

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880677(-;-)
Make rs730880677(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350069
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880677
ebirs730880677
HLIrs730880677
Exacrs730880677
Varsomers730880677
Maprs730880677
PheGenIrs730880677
hapmaprs730880677
1000 genomesrs730880677
hgdprs730880677
ensemblrs730880677
gopubmedrs730880677
geneviewrs730880677
scholarrs730880677
googlers730880677
pharmgkbrs730880677
gwascentralrs730880677
openSNPrs730880677
23andMers730880677
23andMe allrs730880677
SNP Nexus

SNPshotrs730880677
SNPdbers730880677
MSV3drs730880677
GWAS Ctlgrs730880677
Max Magnitude0
ClinVar
Risk rs730880677(;)
Alt rs730880677(;)
Reference rs730880677(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47371620delG
CLNSRC
CLNACC RCV000158410.2,