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rs267606905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606905(A;A)
Make rs267606905(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23387914
GeneMYH6
is asnp
is mentioned by
dbSNPrs267606905
ebirs267606905
HLIrs267606905
Exacrs267606905
Varsomers267606905
Maprs267606905
PheGenIrs267606905
hapmaprs267606905
1000 genomesrs267606905
hgdprs267606905
ensemblrs267606905
gopubmedrs267606905
geneviewrs267606905
scholarrs267606905
googlers267606905
pharmgkbrs267606905
gwascentralrs267606905
openSNPrs267606905
23andMers267606905
23andMe allrs267606905
SNP Nexus

SNPshotrs267606905
SNPdbers267606905
MSV3drs267606905
GWAS Ctlgrs267606905
Max Magnitude0
ClinVar
Risk rs267606905(A;A)
Alt rs267606905(A;A)
Reference rs267606905(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 1EE
Variation info
Gene MYH6
CLNDBN Dilated cardiomyopathy 1EE
Reversed 1
HGVS NC_000014.8:g.23857123C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015215.25,