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rs387907087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907087(C;T)
Make rs387907087(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position126276476
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs387907087
ebirs387907087
HLIrs387907087
Exacrs387907087
Varsomers387907087
Maprs387907087
PheGenIrs387907087
hapmaprs387907087
1000 genomesrs387907087
hgdprs387907087
ensemblrs387907087
gopubmedrs387907087
geneviewrs387907087
scholarrs387907087
googlers387907087
pharmgkbrs387907087
gwascentralrs387907087
openSNPrs387907087
23andMers387907087
23andMe allrs387907087
SNP Nexus

SNPshotrs387907087
SNPdbers387907087
MSV3drs387907087
GWAS Ctlgrs387907087
Max Magnitude0
ClinVar
Risk rs387907087(T;T)
Alt rs387907087(T;T)
Reference rs387907087(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.126146371C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024042.3,