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rs397515505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515505(C;C)
Make rs397515505(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position14325
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs397515505
ebirs397515505
HLIrs397515505
Exacrs397515505
Varsomers397515505
Maprs397515505
PheGenIrs397515505
hapmaprs397515505
1000 genomesrs397515505
hgdprs397515505
ensemblrs397515505
gopubmedrs397515505
geneviewrs397515505
scholarrs397515505
googlers397515505
pharmgkbrs397515505
gwascentralrs397515505
openSNPrs397515505
23andMers397515505
23andMe allrs397515505
SNP Nexus

SNPshotrs397515505
SNPdbers397515505
MSV3drs397515505
GWAS Ctlgrs397515505
Max Magnitude0
ClinVar
Risk rs397515505(C;C)
Alt rs397515505(C;C)
Reference rs397515505(T;T)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND6
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.14325T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000055700.1,