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rs397515504

From SNPedia

Merged intors193302927
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515504(C;C)
Make rs397515504(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position10237
GeneMT-CO3
is asnp
is mentioned by
dbSNPrs397515504
ebirs397515504
HLIrs397515504
Exacrs397515504
Varsomers397515504
Maprs397515504
PheGenIrs397515504
hapmaprs397515504
1000 genomesrs397515504
hgdprs397515504
ensemblrs397515504
gopubmedrs397515504
geneviewrs397515504
scholarrs397515504
googlers397515504
pharmgkbrs397515504
gwascentralrs397515504
openSNPrs397515504
23andMers397515504
23andMe allrs397515504
SNP Nexus

SNPshotrs397515504
SNPdbers397515504
MSV3drs397515504
GWAS Ctlgrs397515504
StatusMerged into rs193302927
Max Magnitude0
ClinVar
Risk rs397515504(C;C)
Alt rs397515504(C;C)
Reference rs397515504(T;T)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND3
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.10237T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000055695.1,