rs1060499535
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1060499535(-;-) |
Make rs1060499535(-;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 50526317 |
Gene | SCO2, TYMP |
is a | snp |
is | mentioned by |
dbSNP | rs1060499535 |
dbSNP (classic) | rs1060499535 |
ClinGen | rs1060499535 |
ebi | rs1060499535 |
HLI | rs1060499535 |
Exac | rs1060499535 |
Gnomad | rs1060499535 |
Varsome | rs1060499535 |
LitVar | rs1060499535 |
Map | rs1060499535 |
PheGenI | rs1060499535 |
Biobank | rs1060499535 |
1000 genomes | rs1060499535 |
hgdp | rs1060499535 |
ensembl | rs1060499535 |
geneview | rs1060499535 |
scholar | rs1060499535 |
rs1060499535 | |
pharmgkb | rs1060499535 |
gwascentral | rs1060499535 |
openSNP | rs1060499535 |
23andMe | rs1060499535 |
SNPshot | rs1060499535 |
SNPdbe | rs1060499535 |
MSV3d | rs1060499535 |
GWAS Ctlg | rs1060499535 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060499535(-;-) |
Alt | rs1060499535(-;-) |
Reference | Rs1060499535(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.50964746delC |
CLNSRC | |
CLNACC | RCV000208695.1, |