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rs869025186

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025186(C;C)
Make rs869025186(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position14498
GeneMT-ND6
is asnp
is mentioned by
dbSNPrs869025186
ebirs869025186
HLIrs869025186
Exacrs869025186
Varsomers869025186
Maprs869025186
PheGenIrs869025186
hapmaprs869025186
1000 genomesrs869025186
hgdprs869025186
ensemblrs869025186
gopubmedrs869025186
geneviewrs869025186
scholarrs869025186
googlers869025186
pharmgkbrs869025186
gwascentralrs869025186
openSNPrs869025186
23andMers869025186
23andMe allrs869025186
SNP Nexus

SNPshotrs869025186
SNPdbers869025186
MSV3drs869025186
GWAS Ctlgrs869025186
Max Magnitude0
ClinVar
Risk rs869025186(C;C)
Alt rs869025186(C;C)
Reference rs869025186(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.14498T>C
CLNSRC
CLNACC RCV000055702.1,