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rs267606894

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606894(A;G)
Make rs267606894(G;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position12770
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs267606894
ebirs267606894
HLIrs267606894
Exacrs267606894
Varsomers267606894
Maprs267606894
PheGenIrs267606894
hapmaprs267606894
1000 genomesrs267606894
hgdprs267606894
ensemblrs267606894
gopubmedrs267606894
geneviewrs267606894
scholarrs267606894
googlers267606894
pharmgkbrs267606894
gwascentralrs267606894
openSNPrs267606894
23andMers267606894
23andMe allrs267606894
SNP Nexus

SNPshotrs267606894
SNPdbers267606894
MSV3drs267606894
GWAS Ctlgrs267606894
GMAF0.0009346
Max Magnitude0
ClinVar
Risk rs267606894(G;G)
Alt rs267606894(G;G)
Reference rs267606894(A;A)
Significance Pathogenic
Disease Juvenile myopathy
Variation info
Gene ND5
CLNDBN Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
Reversed 0
HGVS NC_012920.1:m.12770A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010339.2,