rs556401323
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs556401323(C;T) |
| Make rs556401323(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 11 |
| Position | 126338325 |
| Gene | DCPS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs556401323 |
| dbSNP (classic) | rs556401323 |
| ClinGen | rs556401323 |
| ebi | rs556401323 |
| HLI | rs556401323 |
| Exac | rs556401323 |
| Gnomad | rs556401323 |
| Varsome | rs556401323 |
| LitVar | rs556401323 |
| Map | rs556401323 |
| PheGenI | rs556401323 |
| Biobank | rs556401323 |
| 1000 genomes | rs556401323 |
| hgdp | rs556401323 |
| ensembl | rs556401323 |
| geneview | rs556401323 |
| scholar | rs556401323 |
| rs556401323 | |
| pharmgkb | rs556401323 |
| gwascentral | rs556401323 |
| openSNP | rs556401323 |
| 23andMe | rs556401323 |
| SNPshot | rs556401323 |
| SNPdbe | rs556401323 |
| MSV3d | rs556401323 |
| GWAS Ctlg | rs556401323 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs556401323(T;T) |
| Alt | rs556401323(T;T) |
| Reference | Rs556401323(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DCPS |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.126208220C>T |
| CLNSRC | |
| CLNACC | RCV000492945.1, |
