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rs727503218

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503218(A;A)
Make rs727503218(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47349896
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503218
ebirs727503218
HLIrs727503218
Exacrs727503218
Varsomers727503218
Maprs727503218
PheGenIrs727503218
hapmaprs727503218
1000 genomesrs727503218
hgdprs727503218
ensemblrs727503218
gopubmedrs727503218
geneviewrs727503218
scholarrs727503218
googlers727503218
pharmgkbrs727503218
gwascentralrs727503218
openSNPrs727503218
23andMers727503218
23andMe allrs727503218
SNP Nexus

SNPshotrs727503218
SNPdbers727503218
MSV3drs727503218
GWAS Ctlgrs727503218
Max Magnitude0
ClinVar
Risk rs727503218(A;A)
Alt rs727503218(A;A)
Reference rs727503218(G;G)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN not specified Cardiomyopathy Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47371447C>T
CLNSRC
CLNACC RCV000151165.2, RCV000158292.1, RCV000168747.1,