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rs769167548

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769167548(C;T)
Make rs769167548(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47349788
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs769167548
ebirs769167548
HLIrs769167548
Exacrs769167548
Varsomers769167548
Maprs769167548
PheGenIrs769167548
hapmaprs769167548
1000 genomesrs769167548
hgdprs769167548
ensemblrs769167548
gopubmedrs769167548
geneviewrs769167548
scholarrs769167548
googlers769167548
pharmgkbrs769167548
gwascentralrs769167548
openSNPrs769167548
23andMers769167548
23andMe allrs769167548
SNP Nexus

SNPshotrs769167548
SNPdbers769167548
MSV3drs769167548
GWAS Ctlgrs769167548
Max Magnitude0
ClinVar
Risk rs769167548(T;T)
Alt rs769167548(T;T)
Reference rs769167548(C;C)
Significance Probable-Pathogenic
Disease not provided Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN not provided Familial hypertrophic cardiomyopathy 4
Reversed 0
HGVS NC_000011.9:g.47371339C>T
CLNSRC
CLNACC RCV000172012.1, RCV000201486.1,