rs770694933
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs770694933(-;-) |
| Make rs770694933(-;C) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 11 |
| Position | 22276149 |
| Gene | ANO5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs770694933 |
| dbSNP (classic) | rs770694933 |
| ClinGen | rs770694933 |
| ebi | rs770694933 |
| HLI | rs770694933 |
| Exac | rs770694933 |
| Gnomad | rs770694933 |
| Varsome | rs770694933 |
| LitVar | rs770694933 |
| Map | rs770694933 |
| PheGenI | rs770694933 |
| Biobank | rs770694933 |
| 1000 genomes | rs770694933 |
| hgdp | rs770694933 |
| ensembl | rs770694933 |
| geneview | rs770694933 |
| scholar | rs770694933 |
| rs770694933 | |
| pharmgkb | rs770694933 |
| gwascentral | rs770694933 |
| openSNP | rs770694933 |
| 23andMe | rs770694933 |
| SNPshot | rs770694933 |
| SNPdbe | rs770694933 |
| MSV3d | rs770694933 |
| GWAS Ctlg | rs770694933 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs770694933(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ANO5 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.22297695delC |
| CLNSRC | |
| CLNACC | RCV000313812.1, |
