rs393152
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 1.5 | Increased risk of both PD and AD |
| (A;G) | 1.2 | Slight increased risk of both PD and AD |
| (G;G) | 1.3 | Normal risk of both PD and AD |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 45641777 |
| Gene | CRHR1-IT1, CRHR1-IT1-CRHR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs393152 |
| dbSNP (classic) | rs393152 |
| ClinGen | rs393152 |
| ebi | rs393152 |
| HLI | rs393152 |
| Exac | rs393152 |
| Gnomad | rs393152 |
| Varsome | rs393152 |
| LitVar | rs393152 |
| Map | rs393152 |
| PheGenI | rs393152 |
| Biobank | rs393152 |
| 1000 genomes | rs393152 |
| hgdp | rs393152 |
| ensembl | rs393152 |
| geneview | rs393152 |
| scholar | rs393152 |
| rs393152 | |
| pharmgkb | rs393152 |
| gwascentral | rs393152 |
| openSNP | rs393152 |
| 23andMe | rs393152 |
| SNPshot | rs393152 |
| SNPdbe | rs393152 |
| MSV3d | rs393152 |
| GWAS Ctlg | rs393152 |
| GMAF | 0.2369 |
| Max Magnitude | 1.5 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19915575 ]
|
| Trait | Parkinson's disease |
| Title | Genome-wide association study reveals genetic risk underlying Parkinson's disease |
| Risk Allele | G |
| P-val | 2E-16 |
| Odds Ratio | 1.30 [NR] |
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
[PMID 20070850] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
[PMID 21898123] The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction.
[PMID 25687773] Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.
