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

rs587776434

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776434(A;A)
Make rs587776434(A;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position3890
GeneMT-ND1
is asnp
is mentioned by
dbSNPrs587776434
ebirs587776434
HLIrs587776434
Exacrs587776434
Varsomers587776434
Maprs587776434
PheGenIrs587776434
hapmaprs587776434
1000 genomesrs587776434
hgdprs587776434
ensemblrs587776434
gopubmedrs587776434
geneviewrs587776434
scholarrs587776434
googlers587776434
pharmgkbrs587776434
gwascentralrs587776434
openSNPrs587776434
23andMers587776434
23andMe allrs587776434
SNP Nexus

SNPshotrs587776434
SNPdbers587776434
MSV3drs587776434
GWAS Ctlgrs587776434
Max Magnitude0
ClinVar
Risk rs587776434(A;A)
Alt rs587776434(A;A)
Reference rs587776434(G;G)
Significance Pathogenic
Disease Leigh syndrome
Variation info
Gene ND1
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.3890G>A
CLNSRC
CLNACC RCV000144000.2,