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rs267606913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606913(A;A)
Make rs267606913(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position1815885
GeneNDUFS6
is asnp
is mentioned by
dbSNPrs267606913
ebirs267606913
HLIrs267606913
Exacrs267606913
Varsomers267606913
Maprs267606913
PheGenIrs267606913
hapmaprs267606913
1000 genomesrs267606913
hgdprs267606913
ensemblrs267606913
gopubmedrs267606913
geneviewrs267606913
scholarrs267606913
googlers267606913
pharmgkbrs267606913
gwascentralrs267606913
openSNPrs267606913
23andMers267606913
23andMe allrs267606913
SNP Nexus

SNPshotrs267606913
SNPdbers267606913
MSV3drs267606913
GWAS Ctlgrs267606913
Max Magnitude0
ClinVar
Risk rs267606913(A;A)
Alt rs267606913(A;A)
Reference rs267606913(G;G)
Significance Pathogenic
Disease Mitochondrial complex I deficiency
Variation info
Gene NDUFS6
CLNDBN Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000005.9:g.1815999G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006389.4,