rs757169781
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs757169781(A;T) |
| Make rs757169781(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 6 |
| Position | 44313103 |
| Gene | AARS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757169781 |
| dbSNP (classic) | rs757169781 |
| ClinGen | rs757169781 |
| ebi | rs757169781 |
| HLI | rs757169781 |
| Exac | rs757169781 |
| Gnomad | rs757169781 |
| Varsome | rs757169781 |
| LitVar | rs757169781 |
| Map | rs757169781 |
| PheGenI | rs757169781 |
| Biobank | rs757169781 |
| 1000 genomes | rs757169781 |
| hgdp | rs757169781 |
| ensembl | rs757169781 |
| geneview | rs757169781 |
| scholar | rs757169781 |
| rs757169781 | |
| pharmgkb | rs757169781 |
| gwascentral | rs757169781 |
| openSNP | rs757169781 |
| 23andMe | rs757169781 |
| SNPshot | rs757169781 |
| SNPdbe | rs757169781 |
| MSV3d | rs757169781 |
| GWAS Ctlg | rs757169781 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs757169781(T;T) |
| Alt | rs757169781(T;T) |
| Reference | Rs757169781(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | AARS2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.44280840A>T |
| CLNSRC | |
| CLNACC | RCV000195876.1, |
