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

rs587776433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776433(A;A)
Make rs587776433(A;G)
ReferenceGRCh38 38.1/142
ChromosomeMT
Position3481
GeneMT-ND1
is asnp
is mentioned by
dbSNPrs587776433
ebirs587776433
HLIrs587776433
Exacrs587776433
Varsomers587776433
Maprs587776433
PheGenIrs587776433
hapmaprs587776433
1000 genomesrs587776433
hgdprs587776433
ensemblrs587776433
gopubmedrs587776433
geneviewrs587776433
scholarrs587776433
googlers587776433
pharmgkbrs587776433
gwascentralrs587776433
openSNPrs587776433
23andMers587776433
23andMe allrs587776433
SNP Nexus

SNPshotrs587776433
SNPdbers587776433
MSV3drs587776433
GWAS Ctlgrs587776433
Max Magnitude0
ClinVar
Risk rs587776433(A;A)
Alt rs587776433(A;A)
Reference rs587776433(G;G)
Significance Pathogenic
Disease Leigh syndrome
Variation info
Gene ND1
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.3481G>A
CLNSRC
CLNACC RCV000143999.2,