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rs727503211

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503211(A;A)
Make rs727503211(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346331
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503211
ebirs727503211
HLIrs727503211
Exacrs727503211
Varsomers727503211
Maprs727503211
PheGenIrs727503211
hapmaprs727503211
1000 genomesrs727503211
hgdprs727503211
ensemblrs727503211
gopubmedrs727503211
geneviewrs727503211
scholarrs727503211
googlers727503211
pharmgkbrs727503211
gwascentralrs727503211
openSNPrs727503211
23andMers727503211
23andMe allrs727503211
SNP Nexus

SNPshotrs727503211
SNPdbers727503211
MSV3drs727503211
GWAS Ctlgrs727503211
Max Magnitude0
ClinVar
Risk rs727503211(A;A)
Alt rs727503211(A;A)
Reference rs727503211(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.47367882C>T
CLNSRC
CLNACC RCV000151147.2,