rs1064792878
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Chromosome | 22 |
Position | 50526000 |
Gene | SCO2, TYMP |
is a | snp |
is | mentioned by |
dbSNP | rs1064792878 |
dbSNP (classic) | rs1064792878 |
ClinGen | rs1064792878 |
ebi | rs1064792878 |
HLI | rs1064792878 |
Exac | rs1064792878 |
Gnomad | rs1064792878 |
Varsome | rs1064792878 |
LitVar | rs1064792878 |
Map | rs1064792878 |
PheGenI | rs1064792878 |
Biobank | rs1064792878 |
1000 genomes | rs1064792878 |
hgdp | rs1064792878 |
ensembl | rs1064792878 |
geneview | rs1064792878 |
scholar | rs1064792878 |
rs1064792878 | |
pharmgkb | rs1064792878 |
gwascentral | rs1064792878 |
openSNP | rs1064792878 |
23andMe | rs1064792878 |
SNPshot | rs1064792878 |
SNPdbe | rs1064792878 |
MSV3d | rs1064792878 |
GWAS Ctlg | rs1064792878 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064792878(A;A) |
Alt | rs1064792878(A;A) |
Reference | Rs1064792878(G;G) |
Significance | Pathogenic |
Disease | Mitochondrial DNA depletion syndrome 1 (MNGIE type) |
Variation | info |
Gene | TYMP SCO2 |
CLNDBN | Mitochondrial DNA depletion syndrome 1 (MNGIE type) |
Reversed | 1 |
HGVS | NC_000022.10:g.50964429C>T |
CLNSRC | |
CLNACC | RCV000208711.1, |