rs137941190
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs137941190(C;T) |
| Make rs137941190(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 11 |
| Position | 126345546 |
| Gene | DCPS, ST3GAL4-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137941190 |
| dbSNP (classic) | rs137941190 |
| ClinGen | rs137941190 |
| ebi | rs137941190 |
| HLI | rs137941190 |
| Exac | rs137941190 |
| Gnomad | rs137941190 |
| Varsome | rs137941190 |
| LitVar | rs137941190 |
| Map | rs137941190 |
| PheGenI | rs137941190 |
| Biobank | rs137941190 |
| 1000 genomes | rs137941190 |
| hgdp | rs137941190 |
| ensembl | rs137941190 |
| geneview | rs137941190 |
| scholar | rs137941190 |
| rs137941190 | |
| pharmgkb | rs137941190 |
| gwascentral | rs137941190 |
| openSNP | rs137941190 |
| 23andMe | rs137941190 |
| SNPshot | rs137941190 |
| SNPdbe | rs137941190 |
| MSV3d | rs137941190 |
| GWAS Ctlg | rs137941190 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs137941190(G;G) rs137941190(T;T) |
| Alt | rs137941190(G;G) rs137941190(T;T) |
| Reference | Rs137941190(C;C) |
| Significance | Pathogenic |
| Disease | AL-RAQAD SYNDROME |
| Variation | info |
| Gene | ST3GAL4-AS1 DCPS |
| CLNDBN | AL-RAQAD SYNDROME |
| Reversed | 0 |
| HGVS | NC_000011.9:g.126215441C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000412619.1, |
