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rs397515507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515507(A;A)
Make rs397515507(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position3635
GeneMT-ND1
is asnp
is mentioned by
dbSNPrs397515507
ebirs397515507
HLIrs397515507
Exacrs397515507
Varsomers397515507
Maprs397515507
PheGenIrs397515507
hapmaprs397515507
1000 genomesrs397515507
hgdprs397515507
ensemblrs397515507
gopubmedrs397515507
geneviewrs397515507
scholarrs397515507
googlers397515507
pharmgkbrs397515507
gwascentralrs397515507
openSNPrs397515507
23andMers397515507
23andMe allrs397515507
SNP Nexus

SNPshotrs397515507
SNPdbers397515507
MSV3drs397515507
GWAS Ctlgrs397515507
Max Magnitude0
ClinVar
Risk rs397515507(A;A)
Alt rs397515507(A;A)
Reference rs397515507(G;G)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND1
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.3635G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000055707.1,