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rs797045091

From SNPedia

Merged intors398124308
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045091(-;GAGT)
Make rs797045091(GAGT;GAGT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position126275004
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs797045091
dbSNP (old)rs797045091
ClinGenrs797045091
ebirs797045091
HLIrs797045091
Exacrs797045091
Gnomadrs797045091
Varsomers797045091
Maprs797045091
PheGenIrs797045091
Biobankrs797045091
1000 genomesrs797045091
hgdprs797045091
ensemblrs797045091
gopubmedrs797045091
geneviewrs797045091
scholarrs797045091
googlers797045091
pharmgkbrs797045091
gwascentralrs797045091
openSNPrs797045091
23andMers797045091
23andMe allrs797045091
SNP Nexus

SNPshotrs797045091
SNPdbers797045091
MSV3drs797045091
GWAS Ctlgrs797045091
StatusMerged into rs398124308
Max Magnitude0
ClinVar
Risk rs797045091(GAGT;GAGT)
Alt rs797045091(GAGT;GAGT)
Reference Rs797045091(;)
Significance Pathogenic
Disease not provided Mitochondrial complex I deficiency
Variation info
Gene FOXRED1
CLNDBN not provided Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000011.9:g.126144897_126144900dupAGTG
CLNSRC HGMD
CLNACC RCV000081797.5, RCV000190588.1,