rs753424199
From SNPedia
| Merged into | rs199422137 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (CT;CT) | 0 | common in clinvar |
| Make rs753424199(-;-) |
| Make rs753424199(-;CT) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 1 |
| Position | 197143097 |
| Gene | ASPM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs753424199 |
| dbSNP (classic) | rs753424199 |
| ClinGen | rs753424199 |
| ebi | rs753424199 |
| HLI | rs753424199 |
| Exac | rs753424199 |
| Gnomad | rs753424199 |
| Varsome | rs753424199 |
| LitVar | rs753424199 |
| Map | rs753424199 |
| PheGenI | rs753424199 |
| Biobank | rs753424199 |
| 1000 genomes | rs753424199 |
| hgdp | rs753424199 |
| ensembl | rs753424199 |
| geneview | rs753424199 |
| scholar | rs753424199 |
| rs753424199 | |
| pharmgkb | rs753424199 |
| gwascentral | rs753424199 |
| openSNP | rs753424199 |
| 23andMe | rs753424199 |
| SNPshot | rs753424199 |
| SNPdbe | rs753424199 |
| MSV3d | rs753424199 |
| GWAS Ctlg | rs753424199 |
| Status | Merged into rs199422137 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs753424199(CT;CT) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ASPM |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.197112227_197112228delCT |
| CLNSRC | |
| CLNACC | RCV000219412.1, |
