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rs368765949

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368765949(C;T)
Make rs368765949(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332244
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs368765949
ebirs368765949
HLIrs368765949
Exacrs368765949
Varsomers368765949
Maprs368765949
PheGenIrs368765949
hapmaprs368765949
1000 genomesrs368765949
hgdprs368765949
ensemblrs368765949
gopubmedrs368765949
geneviewrs368765949
scholarrs368765949
googlers368765949
pharmgkbrs368765949
gwascentralrs368765949
openSNPrs368765949
23andMers368765949
23andMe allrs368765949
SNP Nexus

SNPshotrs368765949
SNPdbers368765949
MSV3drs368765949
GWAS Ctlgrs368765949
Max Magnitude0
ClinVar
Risk rs368765949(T;T)
Alt rs368765949(T;T)
Reference rs368765949(C;C)
Significance Other
Disease Cardiomyopathy Familial hypertrophic cardiomyopathy 4 Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy Familial hypertrophic cardiomyopathy 4 Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47353795C>T
CLNSRC
CLNACC RCV000158241.1, RCV000201437.1, RCV000206843.1,