Have questions? Visit https://www.reddit.com/r/SNPedia

rs368121566

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368121566(A;A)
Make rs368121566(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47347480
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs368121566
ebirs368121566
HLIrs368121566
Exacrs368121566
Varsomers368121566
Maprs368121566
PheGenIrs368121566
hapmaprs368121566
1000 genomesrs368121566
hgdprs368121566
ensemblrs368121566
gopubmedrs368121566
geneviewrs368121566
scholarrs368121566
googlers368121566
pharmgkbrs368121566
gwascentralrs368121566
openSNPrs368121566
23andMers368121566
23andMe allrs368121566
SNP Nexus

SNPshotrs368121566
SNPdbers368121566
MSV3drs368121566
GWAS Ctlgrs368121566
Max Magnitude0
ClinVar
Risk rs368121566(A,T;A,T)
Alt rs368121566(A,T;A,T)
Reference rs368121566(C;C)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47369031C>A; NC_000011.9:g.47369031C>T
CLNSRC
CLNACC RCV000149885.1, RCV000158317.1,