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rs727504864

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504864(A;A)
Make rs727504864(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47337712
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504864
ebirs727504864
HLIrs727504864
Exacrs727504864
Varsomers727504864
Maprs727504864
PheGenIrs727504864
hapmaprs727504864
1000 genomesrs727504864
hgdprs727504864
ensemblrs727504864
gopubmedrs727504864
geneviewrs727504864
scholarrs727504864
googlers727504864
pharmgkbrs727504864
gwascentralrs727504864
openSNPrs727504864
23andMers727504864
23andMe allrs727504864
SNP Nexus

SNPshotrs727504864
SNPdbers727504864
MSV3drs727504864
GWAS Ctlgrs727504864
Max Magnitude0
ClinVar
Risk rs727504864(A,T;A,T)
Alt rs727504864(A,T;A,T)
Reference rs727504864(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.47359263G>T
CLNSRC
CLNACC RCV000156224.4, RCV000211805.1,