rs82625
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs82625(A;A) |
| Make rs82625(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 113996371 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs82625 |
| dbSNP (classic) | rs82625 |
| ClinGen | rs82625 |
| ebi | rs82625 |
| HLI | rs82625 |
| Exac | rs82625 |
| Gnomad | rs82625 |
| Varsome | rs82625 |
| LitVar | rs82625 |
| Map | rs82625 |
| PheGenI | rs82625 |
| Biobank | rs82625 |
| 1000 genomes | rs82625 |
| hgdp | rs82625 |
| ensembl | rs82625 |
| geneview | rs82625 |
| scholar | rs82625 |
| rs82625 | |
| pharmgkb | rs82625 |
| gwascentral | rs82625 |
| openSNP | rs82625 |
| 23andMe | rs82625 |
| SNPshot | rs82625 |
| SNPdbe | rs82625 |
| MSV3d | rs82625 |
| GWAS Ctlg | rs82625 |
| GMAF | 0.06703 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22388998 ]
|
| Trait | |
| Title | Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation. |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | None None |
