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rs376736293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376736293(C;T)
Make rs376736293(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341222
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs376736293
dbSNP (old)rs376736293
ClinGenrs376736293
ebirs376736293
HLIrs376736293
Exacrs376736293
Gnomadrs376736293
Varsomers376736293
Maprs376736293
PheGenIrs376736293
Biobankrs376736293
1000 genomesrs376736293
hgdprs376736293
ensemblrs376736293
gopubmedrs376736293
geneviewrs376736293
scholarrs376736293
googlers376736293
pharmgkbrs376736293
gwascentralrs376736293
openSNPrs376736293
23andMers376736293
23andMe allrs376736293
SNP Nexus

SNPshotrs376736293
SNPdbers376736293
MSV3drs376736293
GWAS Ctlgrs376736293
Max Magnitude0
ClinVar
Risk rs376736293(T;T)
Alt rs376736293(T;T)
Reference Rs376736293(C;C)
Significance Pathogenic
Disease not specified Hypertrophic cardiomyopathy Cardiovascular phenotype
Variation info
Gene MYBPC3
CLNDBN not specified Hypertrophic cardiomyopathy Cardiovascular phenotype
Reversed 0
HGVS NC_000011.9:g.47362773C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000035439.3, RCV000172011.2, RCV000245060.1,