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rs727504349

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504349(A;A)
Make rs727504349(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335200
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504349
ebirs727504349
HLIrs727504349
Exacrs727504349
Varsomers727504349
Maprs727504349
PheGenIrs727504349
hapmaprs727504349
1000 genomesrs727504349
hgdprs727504349
ensemblrs727504349
gopubmedrs727504349
geneviewrs727504349
scholarrs727504349
googlers727504349
pharmgkbrs727504349
gwascentralrs727504349
openSNPrs727504349
23andMers727504349
23andMe allrs727504349
SNP Nexus

SNPshotrs727504349
SNPdbers727504349
MSV3drs727504349
GWAS Ctlgrs727504349
Max Magnitude0
ClinVar
Risk rs727504349(A;A)
Alt rs727504349(A;A)
Reference rs727504349(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.47356751C>T
CLNSRC
CLNACC RCV000154470.2,