rs7617877
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7617877(A;A) |
| Make rs7617877(A;G) |
| Make rs7617877(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 28664273 |
| Gene | LINC00693 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7617877 |
| dbSNP (classic) | rs7617877 |
| ClinGen | rs7617877 |
| ebi | rs7617877 |
| HLI | rs7617877 |
| Exac | rs7617877 |
| Gnomad | rs7617877 |
| Varsome | rs7617877 |
| LitVar | rs7617877 |
| Map | rs7617877 |
| PheGenI | rs7617877 |
| Biobank | rs7617877 |
| 1000 genomes | rs7617877 |
| hgdp | rs7617877 |
| ensembl | rs7617877 |
| geneview | rs7617877 |
| scholar | rs7617877 |
| rs7617877 | |
| pharmgkb | rs7617877 |
| gwascentral | rs7617877 |
| openSNP | rs7617877 |
| 23andMe | rs7617877 |
| SNPshot | rs7617877 |
| SNPdbe | rs7617877 |
| MSV3d | rs7617877 |
| GWAS Ctlg | rs7617877 |
| GMAF | 0.3365 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21044948 ]
|
| Trait | |
| Title | Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21 |
| Risk Allele | A |
| P-val | 0.000003 |
| Odds Ratio | 1.2300 [1.13-1.33] |
