Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776442

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776442(C;C)
Make rs587776442(C;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position3928
GeneMT-ND1
is asnp
is mentioned by
dbSNPrs587776442
ebirs587776442
HLIrs587776442
Exacrs587776442
Varsomers587776442
Maprs587776442
PheGenIrs587776442
hapmaprs587776442
1000 genomesrs587776442
hgdprs587776442
ensemblrs587776442
gopubmedrs587776442
geneviewrs587776442
scholarrs587776442
googlers587776442
pharmgkbrs587776442
gwascentralrs587776442
openSNPrs587776442
23andMers587776442
23andMe allrs587776442
SNP Nexus

SNPshotrs587776442
SNPdbers587776442
MSV3drs587776442
GWAS Ctlgrs587776442
Max Magnitude0
ClinVar
Risk rs587776442(C;C)
Alt rs587776442(C;C)
Reference rs587776442(G;G)
Significance Pathogenic
Disease Leigh syndrome
Variation info
Gene ND1
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.3928G>C
CLNSRC
CLNACC RCV000144023.2,