rs369610897
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs369610897(C;G) |
Make rs369610897(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 84449740 |
Gene | SUCLG1 |
is a | snp |
is | mentioned by |
dbSNP | rs369610897 |
dbSNP (classic) | rs369610897 |
ClinGen | rs369610897 |
ebi | rs369610897 |
HLI | rs369610897 |
Exac | rs369610897 |
Gnomad | rs369610897 |
Varsome | rs369610897 |
LitVar | rs369610897 |
Map | rs369610897 |
PheGenI | rs369610897 |
Biobank | rs369610897 |
1000 genomes | rs369610897 |
hgdp | rs369610897 |
ensembl | rs369610897 |
geneview | rs369610897 |
scholar | rs369610897 |
rs369610897 | |
pharmgkb | rs369610897 |
gwascentral | rs369610897 |
openSNP | rs369610897 |
23andMe | rs369610897 |
SNPshot | rs369610897 |
SNPdbe | rs369610897 |
MSV3d | rs369610897 |
GWAS Ctlg | rs369610897 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369610897(G;G) |
Alt | rs369610897(G;G) |
Reference | Rs369610897(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified Mitochondrial DNA depletion syndrome Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) |
Variation | info |
Gene | SUCLG1 |
CLNDBN | not specified Mitochondrial DNA depletion syndrome Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) |
Reversed | 0 |
HGVS | NC_000002.11:g.84676864C>G |
CLNSRC | |
CLNACC | RCV000186193.2, RCV000322795.1, RCV000377493.1, |