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rs727504276

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504276(A;A)
Make rs727504276(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332969
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504276
ebirs727504276
HLIrs727504276
Exacrs727504276
Varsomers727504276
Maprs727504276
PheGenIrs727504276
hapmaprs727504276
1000 genomesrs727504276
hgdprs727504276
ensemblrs727504276
gopubmedrs727504276
geneviewrs727504276
scholarrs727504276
googlers727504276
pharmgkbrs727504276
gwascentralrs727504276
openSNPrs727504276
23andMers727504276
23andMe allrs727504276
SNP Nexus

SNPshotrs727504276
SNPdbers727504276
MSV3drs727504276
GWAS Ctlgrs727504276
Max Magnitude0
ClinVar
Risk rs727504276(A;A)
Alt rs727504276(A;A)
Reference rs727504276(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.47354520C>T
CLNSRC
CLNACC RCV000154279.2,