rs768344665
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs768344665(-;-) |
| Make rs768344665(-;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 12 |
| Position | 32754023 |
| Gene | YARS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs768344665 |
| dbSNP (classic) | rs768344665 |
| ClinGen | rs768344665 |
| ebi | rs768344665 |
| HLI | rs768344665 |
| Exac | rs768344665 |
| Gnomad | rs768344665 |
| Varsome | rs768344665 |
| LitVar | rs768344665 |
| Map | rs768344665 |
| PheGenI | rs768344665 |
| Biobank | rs768344665 |
| 1000 genomes | rs768344665 |
| hgdp | rs768344665 |
| ensembl | rs768344665 |
| geneview | rs768344665 |
| scholar | rs768344665 |
| rs768344665 | |
| pharmgkb | rs768344665 |
| gwascentral | rs768344665 |
| openSNP | rs768344665 |
| 23andMe | rs768344665 |
| SNPshot | rs768344665 |
| SNPdbe | rs768344665 |
| MSV3d | rs768344665 |
| GWAS Ctlg | rs768344665 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs768344665(-;-) |
| Alt | rs768344665(-;-) |
| Reference | Rs768344665(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | YARS2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000012.11:g.32906957delT |
| CLNSRC | |
| CLNACC | RCV000479623.1, |
