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rs869025187

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025187(A;A)
Make rs869025187(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position14279
GeneND6
is asnp
is mentioned by
dbSNPrs869025187
dbSNP (old)rs869025187
ClinGenrs869025187
ebirs869025187
HLIrs869025187
Exacrs869025187
Gnomadrs869025187
Varsomers869025187
Maprs869025187
PheGenIrs869025187
Biobankrs869025187
1000 genomesrs869025187
hgdprs869025187
ensemblrs869025187
gopubmedrs869025187
geneviewrs869025187
scholarrs869025187
googlers869025187
pharmgkbrs869025187
gwascentralrs869025187
openSNPrs869025187
23andMers869025187
23andMe allrs869025187
SNP Nexus

SNPshotrs869025187
SNPdbers869025187
MSV3drs869025187
GWAS Ctlgrs869025187
Max Magnitude0
ClinVar
Risk rs869025187(A;A)
Alt rs869025187(A;A)
Reference Rs869025187(G;G)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND6
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.14279G>A
CLNSRC
CLNACC RCV000055705.1,