rs1491942
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs1491942(C;C) |
| Make rs1491942(C;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 12 |
| Position | 40227006 |
| Gene | LRRK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1491942 |
| dbSNP (classic) | rs1491942 |
| ClinGen | rs1491942 |
| ebi | rs1491942 |
| HLI | rs1491942 |
| Exac | rs1491942 |
| Gnomad | rs1491942 |
| Varsome | rs1491942 |
| LitVar | rs1491942 |
| Map | rs1491942 |
| PheGenI | rs1491942 |
| Biobank | rs1491942 |
| 1000 genomes | rs1491942 |
| hgdp | rs1491942 |
| ensembl | rs1491942 |
| geneview | rs1491942 |
| scholar | rs1491942 |
| rs1491942 | |
| pharmgkb | rs1491942 |
| gwascentral | rs1491942 |
| openSNP | rs1491942 |
| 23andMe | rs1491942 |
| SNPshot | rs1491942 |
| SNPdbe | rs1491942 |
| MSV3d | rs1491942 |
| GWAS Ctlg | rs1491942 |
| GMAF | 0.2741 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21292315 ]
|
| Trait | |
| Title | Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies |
| Risk Allele | G |
| P-val | 6E-14 |
| Odds Ratio | 1.2700 [1.21-1.33] |
| GWAS snp | |
|---|---|
| PMID | [PMID 22438815]
|
| Trait | |
| Title | Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. |
| Risk Allele | |
| P-val | 6E-15 |
| Odds Ratio | 1.1700 None |
[PMID 33574311] Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry.
