rs200781477
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs200781477(C;C) |
| Make rs200781477(C;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 6 |
| Position | 44301382 |
| Gene | AARS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200781477 |
| dbSNP (classic) | rs200781477 |
| ClinGen | rs200781477 |
| ebi | rs200781477 |
| HLI | rs200781477 |
| Exac | rs200781477 |
| Gnomad | rs200781477 |
| Varsome | rs200781477 |
| LitVar | rs200781477 |
| Map | rs200781477 |
| PheGenI | rs200781477 |
| Biobank | rs200781477 |
| 1000 genomes | rs200781477 |
| hgdp | rs200781477 |
| ensembl | rs200781477 |
| geneview | rs200781477 |
| scholar | rs200781477 |
| rs200781477 | |
| pharmgkb | rs200781477 |
| gwascentral | rs200781477 |
| openSNP | rs200781477 |
| 23andMe | rs200781477 |
| SNPshot | rs200781477 |
| SNPdbe | rs200781477 |
| MSV3d | rs200781477 |
| GWAS Ctlg | rs200781477 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs200781477(C;C) rs200781477(T;T) |
| Alt | rs200781477(C;C) rs200781477(T;T) |
| Reference | Rs200781477(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | AARS2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.44269119G>T |
| CLNSRC | |
| CLNACC | RCV000200375.1, |
