rs104893891
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs104893891(A;T) |
| Make rs104893891(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 37815827 |
| Gene | GDNF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104893891 |
| dbSNP (classic) | rs104893891 |
| ClinGen | rs104893891 |
| ebi | rs104893891 |
| HLI | rs104893891 |
| Exac | rs104893891 |
| Gnomad | rs104893891 |
| Varsome | rs104893891 |
| LitVar | rs104893891 |
| Map | rs104893891 |
| PheGenI | rs104893891 |
| Biobank | rs104893891 |
| 1000 genomes | rs104893891 |
| hgdp | rs104893891 |
| ensembl | rs104893891 |
| geneview | rs104893891 |
| scholar | rs104893891 |
| rs104893891 | |
| pharmgkb | rs104893891 |
| gwascentral | rs104893891 |
| openSNP | rs104893891 |
| 23andMe | rs104893891 |
| SNPshot | rs104893891 |
| SNPdbe | rs104893891 |
| MSV3d | rs104893891 |
| GWAS Ctlg | rs104893891 |
| Merged from | Rs121918535 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs104893891(T;T) |
| Alt | rs104893891(T;T) |
| Reference | Rs104893891(A;A) |
| Significance | Other |
| Disease | Hirschsprung disease 3 |
| Variation | info |
| Gene | GDNF |
| CLNDBN | Hirschsprung disease 3 |
| Reversed | 1 |
| HGVS | NC_000005.9:g.37815929T>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000009305.3, |
