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rs200873900

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200873900(A;A)
Make rs200873900(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position11696
GeneMT-ND4
is asnp
is mentioned by
dbSNPrs200873900
ebirs200873900
HLIrs200873900
Exacrs200873900
Varsomers200873900
Maprs200873900
PheGenIrs200873900
hapmaprs200873900
1000 genomesrs200873900
hgdprs200873900
ensemblrs200873900
gopubmedrs200873900
geneviewrs200873900
scholarrs200873900
googlers200873900
pharmgkbrs200873900
gwascentralrs200873900
openSNPrs200873900
23andMers200873900
23andMe allrs200873900
SNP Nexus

SNPshotrs200873900
SNPdbers200873900
MSV3drs200873900
GWAS Ctlgrs200873900
GMAF0.008419
Max Magnitude0
ClinVar
Risk rs200873900(A;A)
Alt rs200873900(A;A)
Reference rs200873900(G;G)
Significance Pathogenic
Disease Leber hereditary optic neuropathy with dystonia Leber's optic atrophy
Variation info
Gene ND4
CLNDBN Leber hereditary optic neuropathy with dystonia Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.11696G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010356.2, RCV000055697.1,