rs61734270
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs61734270(C;T) |
| Make rs61734270(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 20 |
| Position | 49524089 |
| Gene | PTGIS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61734270 |
| dbSNP (classic) | rs61734270 |
| ClinGen | rs61734270 |
| ebi | rs61734270 |
| HLI | rs61734270 |
| Exac | rs61734270 |
| Gnomad | rs61734270 |
| Varsome | rs61734270 |
| LitVar | rs61734270 |
| Map | rs61734270 |
| PheGenI | rs61734270 |
| Biobank | rs61734270 |
| 1000 genomes | rs61734270 |
| hgdp | rs61734270 |
| ensembl | rs61734270 |
| geneview | rs61734270 |
| scholar | rs61734270 |
| rs61734270 | |
| pharmgkb | rs61734270 |
| gwascentral | rs61734270 |
| openSNP | rs61734270 |
| 23andMe | rs61734270 |
| SNPshot | rs61734270 |
| SNPdbe | rs61734270 |
| MSV3d | rs61734270 |
| GWAS Ctlg | rs61734270 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs61734270(T;T) |
| Alt | rs61734270(T;T) |
| Reference | Rs61734270(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Childhood-Onset Schizophrenia |
| Variation | info |
| Gene | PTGIS |
| CLNDBN | Childhood-Onset Schizophrenia |
| Reversed | 0 |
| HGVS | NC_000020.10:g.48140626C>T |
| CLNSRC | |
| CLNACC | RCV000202340.1, |
