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rs367546859

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs367546859(C;T)
Make rs367546859(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23420993
GeneMYH7
is asnp
is mentioned by
dbSNPrs367546859
ebirs367546859
HLIrs367546859
Exacrs367546859
Varsomers367546859
Maprs367546859
PheGenIrs367546859
hapmaprs367546859
1000 genomesrs367546859
hgdprs367546859
ensemblrs367546859
gopubmedrs367546859
geneviewrs367546859
scholarrs367546859
googlers367546859
pharmgkbrs367546859
gwascentralrs367546859
openSNPrs367546859
23andMers367546859
23andMe allrs367546859
SNP Nexus

SNPshotrs367546859
SNPdbers367546859
MSV3drs367546859
GWAS Ctlgrs367546859
Max Magnitude0
ClinVar
Risk rs367546859(T;T)
Alt rs367546859(T;T)
Reference rs367546859(C;C)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23890202C>T
CLNSRC
CLNACC RCV000148706.1,