rs1480597
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs1480597(A;A) |
| Make rs1480597(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 44665661 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1480597 |
| dbSNP (classic) | rs1480597 |
| ClinGen | rs1480597 |
| ebi | rs1480597 |
| HLI | rs1480597 |
| Exac | rs1480597 |
| Gnomad | rs1480597 |
| Varsome | rs1480597 |
| LitVar | rs1480597 |
| Map | rs1480597 |
| PheGenI | rs1480597 |
| Biobank | rs1480597 |
| 1000 genomes | rs1480597 |
| hgdp | rs1480597 |
| ensembl | rs1480597 |
| geneview | rs1480597 |
| scholar | rs1480597 |
| rs1480597 | |
| pharmgkb | rs1480597 |
| gwascentral | rs1480597 |
| openSNP | rs1480597 |
| 23andMe | rs1480597 |
| SNPshot | rs1480597 |
| SNPdbe | rs1480597 |
| MSV3d | rs1480597 |
| GWAS Ctlg | rs1480597 |
| GMAF | 0.1006 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs1480597 |
| PubMedID | [PMID 17052657] |
| Condition | Parkinson's disease |
| Gene | Intergenic |
| Risk Allele | |
| pValue | 2.00E-006 |
| OR | 2.5 |
| 95% CI | 1.67-3.33 |
[PMID 19134182
] MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study.
[PMID 20823317] is-rSNP: a novel technique for in silico regulatory SNP detection.
