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rs727503186

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503186(-;-)
Make rs727503186(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337437
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503186
ebirs727503186
HLIrs727503186
Exacrs727503186
Varsomers727503186
Maprs727503186
PheGenIrs727503186
hapmaprs727503186
1000 genomesrs727503186
hgdprs727503186
ensemblrs727503186
gopubmedrs727503186
geneviewrs727503186
scholarrs727503186
googlers727503186
pharmgkbrs727503186
gwascentralrs727503186
openSNPrs727503186
23andMers727503186
23andMe allrs727503186
SNP Nexus

SNPshotrs727503186
SNPdbers727503186
MSV3drs727503186
GWAS Ctlgrs727503186
Max Magnitude0
ClinVar
Risk rs727503186(;)
Alt rs727503186(;)
Reference rs727503186(C;C)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47358988delG
CLNSRC
CLNACC RCV000151091.1, RCV000158370.1,