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rs267606890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606890(C;C)
Make rs267606890(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position10191
GeneMT-CO3
is asnp
is mentioned by
dbSNPrs267606890
ebirs267606890
HLIrs267606890
Exacrs267606890
Varsomers267606890
Maprs267606890
PheGenIrs267606890
hapmaprs267606890
1000 genomesrs267606890
hgdprs267606890
ensemblrs267606890
gopubmedrs267606890
geneviewrs267606890
scholarrs267606890
googlers267606890
pharmgkbrs267606890
gwascentralrs267606890
openSNPrs267606890
23andMers267606890
23andMe allrs267606890
SNP Nexus

SNPshotrs267606890
SNPdbers267606890
MSV3drs267606890
GWAS Ctlgrs267606890
Max Magnitude0
ClinVar
Risk rs267606890(C;C)
Alt rs267606890(C;C)
Reference rs267606890(T;T)
Significance Pathogenic
Disease Mitochondrial complex I deficiency Leigh syndrome
Variation info
Gene ND3
CLNDBN Mitochondrial complex I deficiency Leigh syndrome
Reversed 0
HGVS NC_012920.1:m.10191T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010358.2, RCV000144010.2,