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rs727504293

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504293(C;T)
Make rs727504293(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47341006
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504293
ebirs727504293
HLIrs727504293
Exacrs727504293
Varsomers727504293
Maprs727504293
PheGenIrs727504293
hapmaprs727504293
1000 genomesrs727504293
hgdprs727504293
ensemblrs727504293
gopubmedrs727504293
geneviewrs727504293
scholarrs727504293
googlers727504293
pharmgkbrs727504293
gwascentralrs727504293
openSNPrs727504293
23andMers727504293
23andMe allrs727504293
SNP Nexus

SNPshotrs727504293
SNPdbers727504293
MSV3drs727504293
GWAS Ctlgrs727504293
Max Magnitude0
ClinVar
Risk rs727504293(T;T)
Alt rs727504293(T;T)
Reference rs727504293(C;C)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47362557G>A
CLNSRC
CLNACC RCV000154308.4, RCV000211801.1,