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rs267606907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606907(A;A)
Make rs267606907(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23396329
GeneMYH6
is asnp
is mentioned by
dbSNPrs267606907
ebirs267606907
HLIrs267606907
Exacrs267606907
Varsomers267606907
Maprs267606907
PheGenIrs267606907
hapmaprs267606907
1000 genomesrs267606907
hgdprs267606907
ensemblrs267606907
gopubmedrs267606907
geneviewrs267606907
scholarrs267606907
googlers267606907
pharmgkbrs267606907
gwascentralrs267606907
openSNPrs267606907
23andMers267606907
23andMe allrs267606907
SNP Nexus

SNPshotrs267606907
SNPdbers267606907
MSV3drs267606907
GWAS Ctlgrs267606907
Max Magnitude0
ClinVar
Risk rs267606907(A;A)
Alt rs267606907(A;A)
Reference rs267606907(G;G)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 14
Variation info
Gene MYH6
CLNDBN Familial hypertrophic cardiomyopathy 14
Reversed 1
HGVS NC_000014.8:g.23865538C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015210.21,