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rs368770848

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368770848(G;T)
Make rs368770848(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343117
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs368770848
ebirs368770848
HLIrs368770848
Exacrs368770848
Varsomers368770848
Maprs368770848
PheGenIrs368770848
hapmaprs368770848
1000 genomesrs368770848
hgdprs368770848
ensemblrs368770848
gopubmedrs368770848
geneviewrs368770848
scholarrs368770848
googlers368770848
pharmgkbrs368770848
gwascentralrs368770848
openSNPrs368770848
23andMers368770848
23andMe allrs368770848
SNP Nexus

SNPshotrs368770848
SNPdbers368770848
MSV3drs368770848
GWAS Ctlgrs368770848
Max Magnitude0
ClinVar
Risk rs368770848(A,T;A,T)
Alt rs368770848(A,T;A,T)
Reference rs368770848(G;G)
Significance Probable-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.47364668G>A
CLNSRC
CLNACC RCV000035381.3, RCV000208312.1,