rs281865467
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs281865467(C;T) |
| Make rs281865467(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 11 |
| Position | 22259649 |
| Gene | ANO5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs281865467 |
| dbSNP (classic) | rs281865467 |
| ClinGen | rs281865467 |
| ebi | rs281865467 |
| HLI | rs281865467 |
| Exac | rs281865467 |
| Gnomad | rs281865467 |
| Varsome | rs281865467 |
| LitVar | rs281865467 |
| Map | rs281865467 |
| PheGenI | rs281865467 |
| Biobank | rs281865467 |
| 1000 genomes | rs281865467 |
| hgdp | rs281865467 |
| ensembl | rs281865467 |
| geneview | rs281865467 |
| scholar | rs281865467 |
| rs281865467 | |
| pharmgkb | rs281865467 |
| gwascentral | rs281865467 |
| openSNP | rs281865467 |
| 23andMe | rs281865467 |
| SNPshot | rs281865467 |
| SNPdbe | rs281865467 |
| MSV3d | rs281865467 |
| GWAS Ctlg | rs281865467 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs281865467(T;T) |
| Alt | rs281865467(T;T) |
| Reference | Rs281865467(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | ANO5 |
| CLNDBN | not specified not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.22281195C>T |
| CLNSRC | |
| CLNACC | RCV000380299.1, RCV000487292.1, |
