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rs397515509

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515509(C;T)
Make rs397515509(T;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position4025
GeneMT-CO1
is asnp
is mentioned by
dbSNPrs397515509
ebirs397515509
HLIrs397515509
Exacrs397515509
Varsomers397515509
Maprs397515509
PheGenIrs397515509
hapmaprs397515509
1000 genomesrs397515509
hgdprs397515509
ensemblrs397515509
gopubmedrs397515509
geneviewrs397515509
scholarrs397515509
googlers397515509
pharmgkbrs397515509
gwascentralrs397515509
openSNPrs397515509
23andMers397515509
23andMe allrs397515509
SNP Nexus

SNPshotrs397515509
SNPdbers397515509
MSV3drs397515509
GWAS Ctlgrs397515509
Max Magnitude0
ClinVar
Risk rs397515509(A,G,T;A,G,T)
Alt rs397515509(A,G,T;A,G,T)
Reference rs397515509(C;C)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND1
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.4025C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055709.1,