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rs267606906

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606906(C;T)
Make rs267606906(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23394264
GeneMYH6
is asnp
is mentioned by
dbSNPrs267606906
ebirs267606906
HLIrs267606906
Exacrs267606906
Varsomers267606906
Maprs267606906
PheGenIrs267606906
hapmaprs267606906
1000 genomesrs267606906
hgdprs267606906
ensemblrs267606906
gopubmedrs267606906
geneviewrs267606906
scholarrs267606906
googlers267606906
pharmgkbrs267606906
gwascentralrs267606906
openSNPrs267606906
23andMers267606906
23andMe allrs267606906
SNP Nexus

SNPshotrs267606906
SNPdbers267606906
MSV3drs267606906
GWAS Ctlgrs267606906
Max Magnitude0
ClinVar
Risk rs267606906(T;T)
Alt rs267606906(T;T)
Reference rs267606906(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1EE
Variation info
Gene MYH6
CLNDBN Dilated cardiomyopathy 1EE
Reversed 1
HGVS NC_000014.8:g.23863473G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015213.25,