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rs199795644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199795644(A;A)
Make rs199795644(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position14831
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs199795644
ebirs199795644
HLIrs199795644
Exacrs199795644
Varsomers199795644
Maprs199795644
PheGenIrs199795644
hapmaprs199795644
1000 genomesrs199795644
hgdprs199795644
ensemblrs199795644
gopubmedrs199795644
geneviewrs199795644
scholarrs199795644
googlers199795644
pharmgkbrs199795644
gwascentralrs199795644
openSNPrs199795644
23andMers199795644
23andMe allrs199795644
SNP Nexus

SNPshotrs199795644
SNPdbers199795644
MSV3drs199795644
GWAS Ctlgrs199795644
Max Magnitude0
ClinVar
Risk rs199795644(A;A)
Alt rs199795644(A;A)
Reference rs199795644(G;G)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene CYTB
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.14831G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000055706.1,