rs9806762
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9806762(A;A) |
| Make rs9806762(A;G) |
| Make rs9806762(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 88118508 |
| Gene | NTRK3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9806762 |
| dbSNP (classic) | rs9806762 |
| ClinGen | rs9806762 |
| ebi | rs9806762 |
| HLI | rs9806762 |
| Exac | rs9806762 |
| Gnomad | rs9806762 |
| Varsome | rs9806762 |
| LitVar | rs9806762 |
| Map | rs9806762 |
| PheGenI | rs9806762 |
| Biobank | rs9806762 |
| 1000 genomes | rs9806762 |
| hgdp | rs9806762 |
| ensembl | rs9806762 |
| geneview | rs9806762 |
| scholar | rs9806762 |
| rs9806762 | |
| pharmgkb | rs9806762 |
| gwascentral | rs9806762 |
| openSNP | rs9806762 |
| 23andMe | rs9806762 |
| SNPshot | rs9806762 |
| SNPdbe | rs9806762 |
| MSV3d | rs9806762 |
| GWAS Ctlg | rs9806762 |
| GMAF | 0.332 |
| 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 | 0.000007 |
| Odds Ratio | None None |
