rs370471013
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs370471013(C;C) |
| Make rs370471013(C;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | MT |
| Position | 5559 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs370471013 |
| dbSNP (classic) | rs370471013 |
| ClinGen | rs370471013 |
| ebi | rs370471013 |
| HLI | rs370471013 |
| Exac | rs370471013 |
| Gnomad | rs370471013 |
| Varsome | rs370471013 |
| LitVar | rs370471013 |
| Map | rs370471013 |
| PheGenI | rs370471013 |
| Biobank | rs370471013 |
| 1000 genomes | rs370471013 |
| hgdp | rs370471013 |
| ensembl | rs370471013 |
| geneview | rs370471013 |
| scholar | rs370471013 |
| rs370471013 | |
| pharmgkb | rs370471013 |
| gwascentral | rs370471013 |
| openSNP | rs370471013 |
| 23andMe | rs370471013 |
| SNPshot | rs370471013 |
| SNPdbe | rs370471013 |
| MSV3d | rs370471013 |
| GWAS Ctlg | rs370471013 |
| Merged from | Rs587776436 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs370471013(C;C) |
| Alt | rs370471013(C;C) |
| Reference | Rs370471013(T;T) |
| Significance | Pathogenic |
| Disease | Leigh syndrome |
| Variation | info |
| Gene | |
| CLNDBN | Leigh syndrome |
| Reversed | 1 |
| HGVS | NC_012920.1:m.5559A>G |
| CLNSRC | |
| CLNACC | RCV000144003.2, |
