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rs267606830

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606830(A;G)
Make rs267606830(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position126277517
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs267606830
ebirs267606830
HLIrs267606830
Exacrs267606830
Varsomers267606830
Maprs267606830
PheGenIrs267606830
hapmaprs267606830
1000 genomesrs267606830
hgdprs267606830
ensemblrs267606830
gopubmedrs267606830
geneviewrs267606830
scholarrs267606830
googlers267606830
pharmgkbrs267606830
gwascentralrs267606830
openSNPrs267606830
23andMers267606830
23andMe allrs267606830
SNP Nexus

SNPshotrs267606830
SNPdbers267606830
MSV3drs267606830
GWAS Ctlgrs267606830
Max Magnitude0
ClinVar
Risk rs267606830(C,G;C,G)
Alt rs267606830(C,G;C,G)
Reference rs267606830(A;A)
Significance Pathogenic
Disease Mitochondrial complex I deficiency
Variation info
Gene FOXRED1
CLNDBN Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000011.9:g.126147412A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000016.4,