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rs727504333

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504333(A;G)
Make rs727504333(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47334012
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504333
ebirs727504333
HLIrs727504333
Exacrs727504333
Varsomers727504333
Maprs727504333
PheGenIrs727504333
hapmaprs727504333
1000 genomesrs727504333
hgdprs727504333
ensemblrs727504333
gopubmedrs727504333
geneviewrs727504333
scholarrs727504333
googlers727504333
pharmgkbrs727504333
gwascentralrs727504333
openSNPrs727504333
23andMers727504333
23andMe allrs727504333
SNP Nexus

SNPshotrs727504333
SNPdbers727504333
MSV3drs727504333
GWAS Ctlgrs727504333
Max Magnitude0
ClinVar
Risk rs727504333(G;G)
Alt rs727504333(G;G)
Reference rs727504333(A;A)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355563T>C
CLNSRC
CLNACC RCV000154442.2,