rs766771165
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Make rs766771165(-;A) |
| Make rs766771165(A;A) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 6 |
| Position | 44307280 |
| Gene | AARS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs766771165 |
| dbSNP (classic) | rs766771165 |
| ClinGen | rs766771165 |
| ebi | rs766771165 |
| HLI | rs766771165 |
| Exac | rs766771165 |
| Gnomad | rs766771165 |
| Varsome | rs766771165 |
| LitVar | rs766771165 |
| Map | rs766771165 |
| PheGenI | rs766771165 |
| Biobank | rs766771165 |
| 1000 genomes | rs766771165 |
| hgdp | rs766771165 |
| ensembl | rs766771165 |
| geneview | rs766771165 |
| scholar | rs766771165 |
| rs766771165 | |
| pharmgkb | rs766771165 |
| gwascentral | rs766771165 |
| openSNP | rs766771165 |
| 23andMe | rs766771165 |
| SNPshot | rs766771165 |
| SNPdbe | rs766771165 |
| MSV3d | rs766771165 |
| GWAS Ctlg | rs766771165 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs766771165(A;A) |
| Alt | rs766771165(A;A) |
| Reference | Rs766771165(-;-) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | AARS2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.44275018dupA |
| CLNSRC | |
| CLNACC | RCV000199735.1, |
