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rs727503176

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503176(C;C)
Make rs727503176(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333920
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503176
ebirs727503176
HLIrs727503176
Exacrs727503176
Varsomers727503176
Maprs727503176
PheGenIrs727503176
hapmaprs727503176
1000 genomesrs727503176
hgdprs727503176
ensemblrs727503176
gopubmedrs727503176
geneviewrs727503176
scholarrs727503176
googlers727503176
pharmgkbrs727503176
gwascentralrs727503176
openSNPrs727503176
23andMers727503176
23andMe allrs727503176
SNP Nexus

SNPshotrs727503176
SNPdbers727503176
MSV3drs727503176
GWAS Ctlgrs727503176
Max Magnitude0
ClinVar
Risk rs727503176(C;C)
Alt rs727503176(C;C)
Reference rs727503176(T;T)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355471A>G
CLNSRC
CLNACC RCV000151078.2,