rs11711441
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11711441(A;A) |
| Make rs11711441(A;G) |
| Make rs11711441(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 183103487 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11711441 |
| dbSNP (classic) | rs11711441 |
| ClinGen | rs11711441 |
| ebi | rs11711441 |
| HLI | rs11711441 |
| Exac | rs11711441 |
| Gnomad | rs11711441 |
| Varsome | rs11711441 |
| LitVar | rs11711441 |
| Map | rs11711441 |
| PheGenI | rs11711441 |
| Biobank | rs11711441 |
| 1000 genomes | rs11711441 |
| hgdp | rs11711441 |
| ensembl | rs11711441 |
| geneview | rs11711441 |
| scholar | rs11711441 |
| rs11711441 | |
| pharmgkb | rs11711441 |
| gwascentral | rs11711441 |
| openSNP | rs11711441 |
| 23andMe | rs11711441 |
| SNPshot | rs11711441 |
| SNPdbe | rs11711441 |
| MSV3d | rs11711441 |
| GWAS Ctlg | rs11711441 |
| GMAF | 0.1433 |
| Max Magnitude | 0 |
| 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 | 8E-12 |
| Odds Ratio | 1.1900 [1.13-1.25] |
[PMID 23496138] MCCC1/LAMP3 reduces risk of sporadic Parkinson's disease in Han Chinese.
