rs10206961
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10206961(C;C) |
| Make rs10206961(C;T) |
| Make rs10206961(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 85587861 |
| Gene | VAMP5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10206961 |
| dbSNP (classic) | rs10206961 |
| ClinGen | rs10206961 |
| ebi | rs10206961 |
| HLI | rs10206961 |
| Exac | rs10206961 |
| Gnomad | rs10206961 |
| Varsome | rs10206961 |
| LitVar | rs10206961 |
| Map | rs10206961 |
| PheGenI | rs10206961 |
| Biobank | rs10206961 |
| 1000 genomes | rs10206961 |
| hgdp | rs10206961 |
| ensembl | rs10206961 |
| geneview | rs10206961 |
| scholar | rs10206961 |
| rs10206961 | |
| pharmgkb | rs10206961 |
| gwascentral | rs10206961 |
| openSNP | rs10206961 |
| 23andMe | rs10206961 |
| SNPshot | rs10206961 |
| SNPdbe | rs10206961 |
| MSV3d | rs10206961 |
| GWAS Ctlg | rs10206961 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26970437] Potential association of VAMP5 polymorphisms with total colonic aganglionosis in Hirschsprung disease.
[PMID 29695640
] Association of VAMP5 and MCC genetic polymorphisms with increased risk of Hirschsprung disease susceptibility in Southern Chinese children.
