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rs387906732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906732(A;G)
Make rs387906732(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position5816
GeneCPOX
is asnp
is mentioned by
dbSNPrs387906732
ebirs387906732
HLIrs387906732
Exacrs387906732
Varsomers387906732
Maprs387906732
PheGenIrs387906732
hapmaprs387906732
1000 genomesrs387906732
hgdprs387906732
ensemblrs387906732
gopubmedrs387906732
geneviewrs387906732
scholarrs387906732
googlers387906732
pharmgkbrs387906732
gwascentralrs387906732
openSNPrs387906732
23andMers387906732
23andMe allrs387906732
SNP Nexus

SNPshotrs387906732
SNPdbers387906732
MSV3drs387906732
GWAS Ctlgrs387906732
Max Magnitude0
ClinVar
Risk rs387906732(G;G)
Alt rs387906732(G;G)
Reference rs387906732(A;A)
Significance Pathogenic
Disease Dystonia
Variation info
Gene
CLNDBN Dystonia, mitochondrial
Reversed 0
HGVS NC_012920.1:m.5816A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022897.2,