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rs267606888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606888(A;A)
Make rs267606888(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position4810
GeneND2
is asnp
is mentioned by
dbSNPrs267606888
dbSNP (old)rs267606888
ClinGenrs267606888
ebirs267606888
HLIrs267606888
Exacrs267606888
Varsomers267606888
Maprs267606888
PheGenIrs267606888
Biobankrs267606888
1000 genomesrs267606888
hgdprs267606888
ensemblrs267606888
gopubmedrs267606888
geneviewrs267606888
scholarrs267606888
googlers267606888
pharmgkbrs267606888
gwascentralrs267606888
openSNPrs267606888
23andMers267606888
23andMe allrs267606888
SNP Nexus

SNPshotrs267606888
SNPdbers267606888
MSV3drs267606888
GWAS Ctlgrs267606888
Max Magnitude0
ClinVar
Risk rs267606888(A;A)
Alt rs267606888(A;A)
Reference Rs267606888(G;G)
Significance Pathogenic
Disease Mitochondrial complex I deficiency
Variation info
Gene ND2
CLNDBN Mitochondrial complex I deficiency
Reversed 0
HGVS NC_012920.1:m.4810G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010368.4,