rs763595926
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (TCAC;TCAC) | 0 | common in clinvar |
| Make rs763595926(-;-) |
| Make rs763595926(-;TCAC) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 20 |
| Position | 44626448 |
| Gene | ADA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs763595926 |
| dbSNP (classic) | rs763595926 |
| ClinGen | rs763595926 |
| ebi | rs763595926 |
| HLI | rs763595926 |
| Exac | rs763595926 |
| Gnomad | rs763595926 |
| Varsome | rs763595926 |
| LitVar | rs763595926 |
| Map | rs763595926 |
| PheGenI | rs763595926 |
| Biobank | rs763595926 |
| 1000 genomes | rs763595926 |
| hgdp | rs763595926 |
| ensembl | rs763595926 |
| geneview | rs763595926 |
| scholar | rs763595926 |
| rs763595926 | |
| pharmgkb | rs763595926 |
| gwascentral | rs763595926 |
| openSNP | rs763595926 |
| 23andMe | rs763595926 |
| SNPshot | rs763595926 |
| SNPdbe | rs763595926 |
| MSV3d | rs763595926 |
| GWAS Ctlg | rs763595926 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs763595926(-;-) |
| Alt | rs763595926(-;-) |
| Reference | Rs763595926(TCAC;TCAC) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ADA |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000020.10:g.43255089_43255092delTCAC |
| CLNSRC | |
| CLNACC | RCV000481952.1, |
