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rs878853830

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853830(-;-)
Make rs878853830(-;T)
Make rs878853830(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47343135
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs878853830
ebirs878853830
HLIrs878853830
Exacrs878853830
Varsomers878853830
Maprs878853830
PheGenIrs878853830
hapmaprs878853830
1000 genomesrs878853830
hgdprs878853830
ensemblrs878853830
gopubmedrs878853830
geneviewrs878853830
scholarrs878853830
googlers878853830
pharmgkbrs878853830
gwascentralrs878853830
openSNPrs878853830
23andMers878853830
23andMe allrs878853830
SNP Nexus

SNPshotrs878853830
SNPdbers878853830
MSV3drs878853830
GWAS Ctlgrs878853830
Max Magnitude0
ClinVar
Risk rs878853830(T;T)
Alt rs878853830(T;T)
Reference rs878853830(;)
Significance Pathogenic
Disease Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364687dupA
CLNSRC
CLNACC RCV000228088.1,