rs1064792857
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (T;T) | 0 | common in clinvar | 
| Chromosome | 22 | 
| Position | 50529564 | 
| Gene | TYMP | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs1064792857 | 
| dbSNP (classic) | rs1064792857 | 
| ClinGen | rs1064792857 | 
| ebi | rs1064792857 | 
| HLI | rs1064792857 | 
| Exac | rs1064792857 | 
| Gnomad | rs1064792857 | 
| Varsome | rs1064792857 | 
| LitVar | rs1064792857 | 
| Map | rs1064792857 | 
| PheGenI | rs1064792857 | 
| Biobank | rs1064792857 | 
| 1000 genomes | rs1064792857 | 
| hgdp | rs1064792857 | 
| ensembl | rs1064792857 | 
| geneview | rs1064792857 | 
| scholar | rs1064792857 | 
| rs1064792857 | |
| pharmgkb | rs1064792857 | 
| gwascentral | rs1064792857 | 
| openSNP | rs1064792857 | 
| 23andMe | rs1064792857 | 
| SNPshot | rs1064792857 | 
| SNPdbe | rs1064792857 | 
| MSV3d | rs1064792857 | 
| GWAS Ctlg | rs1064792857 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs1064792857(G;G) | 
| Alt | rs1064792857(G;G) | 
| Reference | Rs1064792857(T;T) | 
| Significance | Pathogenic | 
| Disease | Mitochondrial DNA depletion syndrome 1 (MNGIE type) | 
| Variation | info | 
| Gene | TYMP | 
| CLNDBN | Mitochondrial DNA depletion syndrome 1 (MNGIE type) | 
| Reversed | 1 | 
| HGVS | NC_000022.10:g.50967993A>C | 
| CLNSRC | |
| CLNACC | RCV000208699.1, | 


