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rs730880687

From SNPedia

Orientationminus
Geno Mag Summary
(CGCG;CGCG) 0 common in clinvar
Make rs730880687(CGCG;GC)
Make rs730880687(GC;GC)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346225
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880687
ebirs730880687
HLIrs730880687
Exacrs730880687
Varsomers730880687
Maprs730880687
PheGenIrs730880687
hapmaprs730880687
1000 genomesrs730880687
hgdprs730880687
ensemblrs730880687
gopubmedrs730880687
geneviewrs730880687
scholarrs730880687
googlers730880687
pharmgkbrs730880687
gwascentralrs730880687
openSNPrs730880687
23andMers730880687
23andMe allrs730880687
SNP Nexus

SNPshotrs730880687
SNPdbers730880687
MSV3drs730880687
GWAS Ctlgrs730880687
Max Magnitude0
ClinVar
Risk rs730880687(GC;GC)
Alt rs730880687(GC;GC)
Reference rs730880687(CGCG;CGCG)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47367776_47367779delCGCGinsGC
CLNSRC
CLNACC RCV000158424.2,