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rs587776436

From SNPedia

Merged intors370471013
Orientationminus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776436(A;G)
Make rs587776436(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position5559
is asnp
is mentioned by
dbSNPrs587776436
ebirs587776436
HLIrs587776436
Exacrs587776436
Varsomers587776436
Maprs587776436
PheGenIrs587776436
hapmaprs587776436
1000 genomesrs587776436
hgdprs587776436
ensemblrs587776436
gopubmedrs587776436
geneviewrs587776436
scholarrs587776436
googlers587776436
pharmgkbrs587776436
gwascentralrs587776436
openSNPrs587776436
23andMers587776436
23andMe allrs587776436
SNP Nexus

SNPshotrs587776436
SNPdbers587776436
MSV3drs587776436
GWAS Ctlgrs587776436
StatusMerged into rs370471013
Max Magnitude0
ClinVar
Risk rs587776436(G;G)
Alt rs587776436(G;G)
Reference rs587776436(A;A)
Significance Pathogenic
Disease Leigh's disease
Variation info
Gene
CLNDBN Leigh's disease
Reversed 0
HGVS NC_012920.1:m.5559A>G
CLNSRC
CLNACC RCV000144003.2,