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rs727503178

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503178(G;T)
Make rs727503178(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333951
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503178
ebirs727503178
HLIrs727503178
Exacrs727503178
Varsomers727503178
Maprs727503178
PheGenIrs727503178
hapmaprs727503178
1000 genomesrs727503178
hgdprs727503178
ensemblrs727503178
gopubmedrs727503178
geneviewrs727503178
scholarrs727503178
googlers727503178
pharmgkbrs727503178
gwascentralrs727503178
openSNPrs727503178
23andMers727503178
23andMe allrs727503178
SNP Nexus

SNPshotrs727503178
SNPdbers727503178
MSV3drs727503178
GWAS Ctlgrs727503178
Max Magnitude0
ClinVar
Risk rs727503178(T;T)
Alt rs727503178(T;T)
Reference rs727503178(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.47355502C>A
CLNSRC
CLNACC RCV000151080.2,