rs138119149
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs138119149(A;A) |
| Make rs138119149(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 44304512 |
| Gene | AARS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs138119149 |
| dbSNP (classic) | rs138119149 |
| ClinGen | rs138119149 |
| ebi | rs138119149 |
| HLI | rs138119149 |
| Exac | rs138119149 |
| Gnomad | rs138119149 |
| Varsome | rs138119149 |
| LitVar | rs138119149 |
| Map | rs138119149 |
| PheGenI | rs138119149 |
| Biobank | rs138119149 |
| 1000 genomes | rs138119149 |
| hgdp | rs138119149 |
| ensembl | rs138119149 |
| geneview | rs138119149 |
| scholar | rs138119149 |
| rs138119149 | |
| pharmgkb | rs138119149 |
| gwascentral | rs138119149 |
| openSNP | rs138119149 |
| 23andMe | rs138119149 |
| SNPshot | rs138119149 |
| SNPdbe | rs138119149 |
| MSV3d | rs138119149 |
| GWAS Ctlg | rs138119149 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs138119149(A;A) |
| Alt | rs138119149(A;A) |
| Reference | Rs138119149(G;G) |
| Significance | Pathogenic |
| Disease | Combined oxidative phosphorylation deficiency 8 not provided |
| Variation | info |
| Gene | AARS2 |
| CLNDBN | Combined oxidative phosphorylation deficiency 8 not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.44272249G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000023929.3, RCV000196012.2, |
