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rs730880668

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880668(-;-)
Make rs730880668(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333307
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880668
ebirs730880668
HLIrs730880668
Exacrs730880668
Varsomers730880668
Maprs730880668
PheGenIrs730880668
hapmaprs730880668
1000 genomesrs730880668
hgdprs730880668
ensemblrs730880668
gopubmedrs730880668
geneviewrs730880668
scholarrs730880668
googlers730880668
pharmgkbrs730880668
gwascentralrs730880668
openSNPrs730880668
23andMers730880668
23andMe allrs730880668
SNP Nexus

SNPshotrs730880668
SNPdbers730880668
MSV3drs730880668
GWAS Ctlgrs730880668
Max Magnitude0
ClinVar
Risk rs730880668(;)
Alt rs730880668(;)
Reference rs730880668(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47354858delG
CLNSRC
CLNACC RCV000158393.1,