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rs267606904

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606904(C;C)
Make rs267606904(C;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23392968
GeneMYH6
is asnp
is mentioned by
dbSNPrs267606904
ebirs267606904
HLIrs267606904
Exacrs267606904
Varsomers267606904
Maprs267606904
PheGenIrs267606904
hapmaprs267606904
1000 genomesrs267606904
hgdprs267606904
ensemblrs267606904
gopubmedrs267606904
geneviewrs267606904
scholarrs267606904
googlers267606904
pharmgkbrs267606904
gwascentralrs267606904
openSNPrs267606904
23andMers267606904
23andMe allrs267606904
SNP Nexus

SNPshotrs267606904
SNPdbers267606904
MSV3drs267606904
GWAS Ctlgrs267606904
Max Magnitude0
ClinVar
Risk rs267606904(C;C)
Alt rs267606904(C;C)
Reference rs267606904(G;G)
Significance Other
Disease Familial hypertrophic cardiomyopathy 14 not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH6
CLNDBN Familial hypertrophic cardiomyopathy 14 not specified Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23862177C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015212.26, RCV000037469.3, RCV000171836.1,