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rs727503219

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503219(C;C)
Make rs727503219(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350009
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503219
ebirs727503219
HLIrs727503219
Exacrs727503219
Varsomers727503219
Maprs727503219
PheGenIrs727503219
hapmaprs727503219
1000 genomesrs727503219
hgdprs727503219
ensemblrs727503219
gopubmedrs727503219
geneviewrs727503219
scholarrs727503219
googlers727503219
pharmgkbrs727503219
gwascentralrs727503219
openSNPrs727503219
23andMers727503219
23andMe allrs727503219
SNP Nexus

SNPshotrs727503219
SNPdbers727503219
MSV3drs727503219
GWAS Ctlgrs727503219
Max Magnitude0
ClinVar
Risk rs727503219(C;C)
Alt rs727503219(C;C)
Reference rs727503219(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47371560C>G
CLNSRC
CLNACC RCV000151167.2,