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rs267606899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606899(C;T)
Make rs267606899(T;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position12848
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs267606899
ebirs267606899
HLIrs267606899
Exacrs267606899
Varsomers267606899
Maprs267606899
PheGenIrs267606899
hapmaprs267606899
1000 genomesrs267606899
hgdprs267606899
ensemblrs267606899
gopubmedrs267606899
geneviewrs267606899
scholarrs267606899
googlers267606899
pharmgkbrs267606899
gwascentralrs267606899
openSNPrs267606899
23andMers267606899
23andMe allrs267606899
SNP Nexus

SNPshotrs267606899
SNPdbers267606899
MSV3drs267606899
GWAS Ctlgrs267606899
Max Magnitude0
ClinVar
Risk rs267606899(T;T)
Alt rs267606899(T;T)
Reference rs267606899(C;C)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND5
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.12848C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010350.2,