rs797045091
From SNPedia
Merged into | rs398124308 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs797045091(-;GAGT) |
Make rs797045091(GAGT;GAGT) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 126275004 |
Gene | FOXRED1 |
is a | snp |
is | mentioned by |
dbSNP | rs797045091 |
dbSNP (classic) | rs797045091 |
ClinGen | rs797045091 |
ebi | rs797045091 |
HLI | rs797045091 |
Exac | rs797045091 |
Gnomad | rs797045091 |
Varsome | rs797045091 |
LitVar | rs797045091 |
Map | rs797045091 |
PheGenI | rs797045091 |
Biobank | rs797045091 |
1000 genomes | rs797045091 |
hgdp | rs797045091 |
ensembl | rs797045091 |
geneview | rs797045091 |
scholar | rs797045091 |
rs797045091 | |
pharmgkb | rs797045091 |
gwascentral | rs797045091 |
openSNP | rs797045091 |
23andMe | rs797045091 |
SNPshot | rs797045091 |
SNPdbe | rs797045091 |
MSV3d | rs797045091 |
GWAS Ctlg | rs797045091 |
Status | Merged into rs398124308 |
Max Magnitude | 0 |
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, |