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rs368104687

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368104687(C;T)
Make rs368104687(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337783
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs368104687
ebirs368104687
HLIrs368104687
Exacrs368104687
Varsomers368104687
Maprs368104687
PheGenIrs368104687
hapmaprs368104687
1000 genomesrs368104687
hgdprs368104687
ensemblrs368104687
gopubmedrs368104687
geneviewrs368104687
scholarrs368104687
googlers368104687
pharmgkbrs368104687
gwascentralrs368104687
openSNPrs368104687
23andMers368104687
23andMe allrs368104687
SNP Nexus

SNPshotrs368104687
SNPdbers368104687
MSV3drs368104687
GWAS Ctlgrs368104687
Max Magnitude0
ClinVar
Risk rs368104687(T;T)
Alt rs368104687(T;T)
Reference rs368104687(C;C)
Significance Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47359334C>T
CLNSRC
CLNACC RCV000035486.2, RCV000148678.1,