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rs267606910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606910(A;A)
Make rs267606910(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23431589
GeneMYH7
is asnp
is mentioned by
dbSNPrs267606910
ebirs267606910
HLIrs267606910
Exacrs267606910
Varsomers267606910
Maprs267606910
PheGenIrs267606910
hapmaprs267606910
1000 genomesrs267606910
hgdprs267606910
ensemblrs267606910
gopubmedrs267606910
geneviewrs267606910
scholarrs267606910
googlers267606910
pharmgkbrs267606910
gwascentralrs267606910
openSNPrs267606910
23andMers267606910
23andMe allrs267606910
SNP Nexus

SNPshotrs267606910
SNPdbers267606910
MSV3drs267606910
GWAS Ctlgrs267606910
Max Magnitude0
ClinVar
Risk rs267606910(A;A)
Alt rs267606910(A;A)
Reference rs267606910(G;G)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 1 Left ventricular noncompaction 5 not specified
Variation info
Gene MYH7
CLNDBN Familial hypertrophic cardiomyopathy 1 Left ventricular noncompaction 5 not specified
Reversed 1
HGVS NC_000014.8:g.23900798C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015186.25, RCV000015187.25, RCV000158756.2,