rs142426358
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs142426358(C;C) |
| Make rs142426358(C;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 37814375 |
| Gene | GDNF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs142426358 |
| dbSNP (classic) | rs142426358 |
| ClinGen | rs142426358 |
| ebi | rs142426358 |
| HLI | rs142426358 |
| Exac | rs142426358 |
| Gnomad | rs142426358 |
| Varsome | rs142426358 |
| LitVar | rs142426358 |
| Map | rs142426358 |
| PheGenI | rs142426358 |
| Biobank | rs142426358 |
| 1000 genomes | rs142426358 |
| hgdp | rs142426358 |
| ensembl | rs142426358 |
| geneview | rs142426358 |
| scholar | rs142426358 |
| rs142426358 | |
| pharmgkb | rs142426358 |
| gwascentral | rs142426358 |
| openSNP | rs142426358 |
| 23andMe | rs142426358 |
| SNPshot | rs142426358 |
| SNPdbe | rs142426358 |
| MSV3d | rs142426358 |
| GWAS Ctlg | rs142426358 |
| Max Magnitude | 0 |
[PMID 24997227] New alterations at potentially regulated regions of the Glial Derived Neurotrophic Factor gene in bipolar disorder
| ClinVar | |
|---|---|
| Risk | rs142426358(C;C) |
| Alt | rs142426358(C;C) |
| Reference | Rs142426358(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Hirschsprung Disease |
| Variation | info |
| Gene | GDNF |
| CLNDBN | Hirschsprung Disease, Dominant |
| Reversed | 0 |
| HGVS | NC_000005.9:g.37814477T>C |
| CLNSRC | |
| CLNACC | RCV000326850.1, |
