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rs727503166

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503166(-;-)
Make rs727503166(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332110
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503166
ebirs727503166
HLIrs727503166
Exacrs727503166
Varsomers727503166
Maprs727503166
PheGenIrs727503166
hapmaprs727503166
1000 genomesrs727503166
hgdprs727503166
ensemblrs727503166
gopubmedrs727503166
geneviewrs727503166
scholarrs727503166
googlers727503166
pharmgkbrs727503166
gwascentralrs727503166
openSNPrs727503166
23andMers727503166
23andMe allrs727503166
SNP Nexus

SNPshotrs727503166
SNPdbers727503166
MSV3drs727503166
GWAS Ctlgrs727503166
Max Magnitude0
ClinVar
Risk rs727503166(;)
Alt rs727503166(;)
Reference rs727503166(A;A)
Significance Pathogenic
Disease Cardiomyopathy not provided Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy not provided Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47353661delT
CLNSRC
CLNACC RCV000151057.1, RCV000158409.1, RCV000168827.1,