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rs587780529

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780529(A;A)
Make rs587780529(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeMT
Position10134
GeneMT-ND3
is asnp
is mentioned by
dbSNPrs587780529
ebirs587780529
HLIrs587780529
Exacrs587780529
Varsomers587780529
Maprs587780529
PheGenIrs587780529
hapmaprs587780529
1000 genomesrs587780529
hgdprs587780529
ensemblrs587780529
gopubmedrs587780529
geneviewrs587780529
scholarrs587780529
googlers587780529
pharmgkbrs587780529
gwascentralrs587780529
openSNPrs587780529
23andMers587780529
23andMe allrs587780529
SNP Nexus

SNPshotrs587780529
SNPdbers587780529
MSV3drs587780529
GWAS Ctlgrs587780529
Max Magnitude0
ClinVar
Risk rs587780529(A;A)
Alt rs587780529(A;A)
Reference rs587780529(C;C)
Significance Pathogenic
Disease Leigh syndrome
Variation info
Gene ND3
CLNDBN Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.10134C>A
CLNSRC
CLNACC RCV000144458.1,