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rs587776438

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776438(A;A)
Make rs587776438(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position10254
GeneND3
is asnp
is mentioned by
dbSNPrs587776438
dbSNP (old)rs587776438
ClinGenrs587776438
ebirs587776438
HLIrs587776438
Exacrs587776438
Gnomadrs587776438
Varsomers587776438
Maprs587776438
PheGenIrs587776438
Biobankrs587776438
1000 genomesrs587776438
hgdprs587776438
ensemblrs587776438
gopubmedrs587776438
geneviewrs587776438
scholarrs587776438
googlers587776438
pharmgkbrs587776438
gwascentralrs587776438
openSNPrs587776438
23andMers587776438
23andMe allrs587776438
SNP Nexus

SNPshotrs587776438
SNPdbers587776438
MSV3drs587776438
GWAS Ctlgrs587776438
Max Magnitude0
ClinVar
Risk rs587776438(A;A)
Alt rs587776438(A;A)
Reference Rs587776438(G;G)
Significance Pathogenic
Disease Leigh syndrome
Variation info
Gene ND3
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.10254G>A
CLNSRC
CLNACC RCV000144012.2,