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rs267606829

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606829(C;T)
Make rs267606829(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position126275389
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs267606829
ebirs267606829
HLIrs267606829
Exacrs267606829
Varsomers267606829
Maprs267606829
PheGenIrs267606829
hapmaprs267606829
1000 genomesrs267606829
hgdprs267606829
ensemblrs267606829
gopubmedrs267606829
geneviewrs267606829
scholarrs267606829
googlers267606829
pharmgkbrs267606829
gwascentralrs267606829
openSNPrs267606829
23andMers267606829
23andMe allrs267606829
SNP Nexus

SNPshotrs267606829
SNPdbers267606829
MSV3drs267606829
GWAS Ctlgrs267606829
Max Magnitude0
ClinVar
Risk rs267606829(T;T)
Alt rs267606829(T;T)
Reference rs267606829(C;C)
Significance Pathogenic
Disease Mitochondrial complex I deficiency
Variation info
Gene FOXRED1
CLNDBN Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000011.9:g.126145284C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000015.4,