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rs387906426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906426(A;A)
Make rs387906426(A;C)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position4640
GenePFDN5
is asnp
is mentioned by
dbSNPrs387906426
ebirs387906426
HLIrs387906426
Exacrs387906426
Varsomers387906426
Maprs387906426
PheGenIrs387906426
hapmaprs387906426
1000 genomesrs387906426
hgdprs387906426
ensemblrs387906426
gopubmedrs387906426
geneviewrs387906426
scholarrs387906426
googlers387906426
pharmgkbrs387906426
gwascentralrs387906426
openSNPrs387906426
23andMers387906426
23andMe allrs387906426
SNP Nexus

SNPshotrs387906426
SNPdbers387906426
MSV3drs387906426
GWAS Ctlgrs387906426
Max Magnitude0
ClinVar
Risk rs387906426(A;A)
Alt rs387906426(A;A)
Reference rs387906426(C;C)
Significance Pathogenic
Disease Leber's optic atrophy
Variation info
Gene ND2
CLNDBN Leber's optic atrophy
Reversed 0
HGVS NC_012920.1:m.4640C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010366.2,