rs11558261
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | carrier for Alpha-1 Antitrypsin Deficiency |
| (G;G) | 0 | common in complete genomics |
| Make rs11558261(A;A) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 94382823 |
| Gene | SERPINA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11558261 |
| dbSNP (classic) | rs11558261 |
| ClinGen | rs11558261 |
| ebi | rs11558261 |
| HLI | rs11558261 |
| Exac | rs11558261 |
| Gnomad | rs11558261 |
| Varsome | rs11558261 |
| LitVar | rs11558261 |
| Map | rs11558261 |
| PheGenI | rs11558261 |
| Biobank | rs11558261 |
| 1000 genomes | rs11558261 |
| hgdp | rs11558261 |
| ensembl | rs11558261 |
| geneview | rs11558261 |
| scholar | rs11558261 |
| rs11558261 | |
| pharmgkb | rs11558261 |
| gwascentral | rs11558261 |
| openSNP | rs11558261 |
| 23andMe | rs11558261 |
| SNPshot | rs11558261 |
| SNPdbe | rs11558261 |
| MSV3d | rs11558261 |
| GWAS Ctlg | rs11558261 |
| Merged from | Rs28931571 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs11558261(A;A) |
| Alt | rs11558261(A;A) |
| Reference | Rs11558261(G;G) |
| Significance | Other |
| Disease | PI NULL(DEVON) PI Q0(DEVON) PI NULL(NEWPORT) PI Q0(NEWPORT) |
| Variation | info |
| Gene | SERPINA1 |
| CLNDBN | PI NULL(DEVON) PI Q0(DEVON) PI NULL(NEWPORT) PI Q0(NEWPORT) |
| Reversed | 1 |
| HGVS | NC_000014.8:g.94849160C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000019597.4, RCV000019598.4, RCV000019599.4, RCV000019600.4, |
