rs11931074
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs11931074(G;T) |
| Make rs11931074(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 89718364 |
| Gene | LOC105377329 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11931074 |
| dbSNP (classic) | rs11931074 |
| ClinGen | rs11931074 |
| ebi | rs11931074 |
| HLI | rs11931074 |
| Exac | rs11931074 |
| Gnomad | rs11931074 |
| Varsome | rs11931074 |
| LitVar | rs11931074 |
| Map | rs11931074 |
| PheGenI | rs11931074 |
| Biobank | rs11931074 |
| 1000 genomes | rs11931074 |
| hgdp | rs11931074 |
| ensembl | rs11931074 |
| geneview | rs11931074 |
| scholar | rs11931074 |
| rs11931074 | |
| pharmgkb | rs11931074 |
| gwascentral | rs11931074 |
| openSNP | rs11931074 |
| 23andMe | rs11931074 |
| SNPshot | rs11931074 |
| SNPdbe | rs11931074 |
| MSV3d | rs11931074 |
| GWAS Ctlg | rs11931074 |
| GMAF | 0.3545 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19915576] |
| Trait | Parkinson's disease |
| Title | Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease |
| Risk Allele | G |
| P-val | 7E-17 |
| Odds Ratio | 1.37 [1.27-1.48] |
[PMID 21853288] Variant in the 3' region of SNCA associated with Parkinson's disease and serum ?-synuclein levels.
[PMID 19063963
] Genetic susceptibility in Parkinson's disease.
[PMID 19771175] Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.
[PMID 19915575] Genome-wide association study reveals genetic risk underlying Parkinson's disease.
[PMID 20070850] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
[PMID 20413655] Genetics of neurodegenerative diseases: insights from high-throughput resequencing.
[PMID 21391235] Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
[PMID 23182315] Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: A replication study in a Taiwanese cohort
[PMID 23820587] Alzheimer's disease and Parkinson's disease genome-wide association study top hits and risk of Parkinson's disease in Korean population
[PMID 23853107] Analysis of genome-wide association study-linked loci in Parkinson's disease of Mainland China
[PMID 23962496] The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
[PMID 25427997] SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population
[PMID 25656566] Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: A meta-analysis
[PMID 25921825] Hyposmia correlates with SNCA variant and non-motor symptoms in Chinese patients with Parkinson's disease
[PMID 28676755] Variants in SNCA Gene Are Associated with Parkinson's Disease Risk and Cognitive Symptoms in a Brazilian Sample.
[PMID 28979204] Hyposmia Is Associated with RBD for PD Patients with Variants of SNCA.
[PMID 30410434] A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease.
