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rs727503204

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503204(A;A)
Make rs727503204(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343020
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503204
ebirs727503204
HLIrs727503204
Exacrs727503204
Varsomers727503204
Maprs727503204
PheGenIrs727503204
hapmaprs727503204
1000 genomesrs727503204
hgdprs727503204
ensemblrs727503204
gopubmedrs727503204
geneviewrs727503204
scholarrs727503204
googlers727503204
pharmgkbrs727503204
gwascentralrs727503204
openSNPrs727503204
23andMers727503204
23andMe allrs727503204
SNP Nexus

SNPshotrs727503204
SNPdbers727503204
MSV3drs727503204
GWAS Ctlgrs727503204
Max Magnitude0
ClinVar
Risk rs727503204(A;A)
Alt rs727503204(A;A)
Reference rs727503204(G;G)
Significance Pathogenic
Disease Cardiomyopathy Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364571C>T
CLNSRC
CLNACC RCV000151139.1, RCV000208143.1,