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rs267606881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606881(A;A)
Make rs267606881(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position8529
GeneMT-ATP6
is asnp
is mentioned by
dbSNPrs267606881
ebirs267606881
HLIrs267606881
Exacrs267606881
Varsomers267606881
Maprs267606881
PheGenIrs267606881
hapmaprs267606881
1000 genomesrs267606881
hgdprs267606881
ensemblrs267606881
gopubmedrs267606881
geneviewrs267606881
scholarrs267606881
googlers267606881
pharmgkbrs267606881
gwascentralrs267606881
openSNPrs267606881
23andMers267606881
23andMe allrs267606881
SNP Nexus

SNPshotrs267606881
SNPdbers267606881
MSV3drs267606881
GWAS Ctlgrs267606881
Max Magnitude0
ClinVar
Risk rs267606881(A;A)
Alt rs267606881(A;A)
Reference rs267606881(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene ATP6
CLNDBN Cardiomyopathy, apical hypertrophic, and neuropathy
Reversed 0
HGVS NC_012920.1:m.8529G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010271.2,