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rs727504345

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504345(C;T)
Make rs727504345(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337460
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504345
ebirs727504345
HLIrs727504345
Exacrs727504345
Varsomers727504345
Maprs727504345
PheGenIrs727504345
hapmaprs727504345
1000 genomesrs727504345
hgdprs727504345
ensemblrs727504345
gopubmedrs727504345
geneviewrs727504345
scholarrs727504345
googlers727504345
pharmgkbrs727504345
gwascentralrs727504345
openSNPrs727504345
23andMers727504345
23andMe allrs727504345
SNP Nexus

SNPshotrs727504345
SNPdbers727504345
MSV3drs727504345
GWAS Ctlgrs727504345
Max Magnitude0
ClinVar
Risk rs727504345(G,T;G,T)
Alt rs727504345(G,T;G,T)
Reference rs727504345(C;C)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47359011G>A; NC_000011.9:g.47359011G>C
CLNSRC
CLNACC RCV000154465.2, RCV000158165.1,