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rs199476106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199476106(A;G)
Make rs199476106(G;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position14495
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs199476106
ebirs199476106
HLIrs199476106
Exacrs199476106
Varsomers199476106
Maprs199476106
PheGenIrs199476106
hapmaprs199476106
1000 genomesrs199476106
hgdprs199476106
ensemblrs199476106
gopubmedrs199476106
geneviewrs199476106
scholarrs199476106
googlers199476106
pharmgkbrs199476106
gwascentralrs199476106
openSNPrs199476106
23andMers199476106
23andMe allrs199476106
SNP Nexus

SNPshotrs199476106
SNPdbers199476106
MSV3drs199476106
GWAS Ctlgrs199476106
Max Magnitude0
ClinVar
Risk rs199476106(G;G)
Alt rs199476106(G;G)
Reference rs199476106(A;A)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND6
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.14495A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010330.2,