rs1044894207
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 21 |
| Position | 43776268 |
| Gene | CSTB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1044894207 |
| dbSNP (classic) | rs1044894207 |
| ClinGen | rs1044894207 |
| ebi | rs1044894207 |
| HLI | rs1044894207 |
| Exac | rs1044894207 |
| Gnomad | rs1044894207 |
| Varsome | rs1044894207 |
| LitVar | rs1044894207 |
| Map | rs1044894207 |
| PheGenI | rs1044894207 |
| Biobank | rs1044894207 |
| 1000 genomes | rs1044894207 |
| hgdp | rs1044894207 |
| ensembl | rs1044894207 |
| geneview | rs1044894207 |
| scholar | rs1044894207 |
| rs1044894207 | |
| pharmgkb | rs1044894207 |
| gwascentral | rs1044894207 |
| openSNP | rs1044894207 |
| 23andMe | rs1044894207 |
| SNPshot | rs1044894207 |
| SNPdbe | rs1044894207 |
| MSV3d | rs1044894207 |
| GWAS Ctlg | rs1044894207 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1044894207(AT;AT) |
| Alt | rs1044894207(AT;AT) |
| Reference | Rs1044894207(-;-) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CSTB |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000021.8:g.45196149_45196150insAT |
| CLNSRC | |
| CLNACC | RCV000485922.1, |
