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rs730880657

From SNPedia

Orientationminus
Geno Mag Summary
(CTACAGCGTGG;CTACAGCGTGG) 0 common in clinvar
Make rs730880657(-;-)
Make rs730880657(-;CTACAGCGTGG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335895
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880657
ebirs730880657
HLIrs730880657
Exacrs730880657
Varsomers730880657
Maprs730880657
PheGenIrs730880657
hapmaprs730880657
1000 genomesrs730880657
hgdprs730880657
ensemblrs730880657
gopubmedrs730880657
geneviewrs730880657
scholarrs730880657
googlers730880657
pharmgkbrs730880657
gwascentralrs730880657
openSNPrs730880657
23andMers730880657
23andMe allrs730880657
SNP Nexus

SNPshotrs730880657
SNPdbers730880657
MSV3drs730880657
GWAS Ctlgrs730880657
Max Magnitude0
ClinVar
Risk rs730880657(;)
Alt rs730880657(;)
Reference rs730880657(CTACAGCGTGG;CTACAGCGTGG)
Significance Pathogenic
Disease not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47357446_47357456delCCACGCTGTAG
CLNSRC
CLNACC RCV000158374.2, RCV000219906.1,