rs529961953
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs529961953(A;A) |
| Make rs529961953(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 11 |
| Position | 22257738 |
| Gene | ANO5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs529961953 |
| dbSNP (classic) | rs529961953 |
| ClinGen | rs529961953 |
| ebi | rs529961953 |
| HLI | rs529961953 |
| Exac | rs529961953 |
| Gnomad | rs529961953 |
| Varsome | rs529961953 |
| LitVar | rs529961953 |
| Map | rs529961953 |
| PheGenI | rs529961953 |
| Biobank | rs529961953 |
| 1000 genomes | rs529961953 |
| hgdp | rs529961953 |
| ensembl | rs529961953 |
| geneview | rs529961953 |
| scholar | rs529961953 |
| rs529961953 | |
| pharmgkb | rs529961953 |
| gwascentral | rs529961953 |
| openSNP | rs529961953 |
| 23andMe | rs529961953 |
| SNPshot | rs529961953 |
| SNPdbe | rs529961953 |
| MSV3d | rs529961953 |
| GWAS Ctlg | rs529961953 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs529961953(A;A) |
| Alt | rs529961953(A;A) |
| Reference | Rs529961953(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ANO5 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.22279284C>A |
| CLNSRC | |
| CLNACC | RCV000438945.1, |
