rs356186
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs356186(A;A) |
Make rs356186(A;G) |
Make rs356186(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 89784213 |
Gene | SNCA |
is a | snp |
is | mentioned by |
dbSNP | rs356186 |
dbSNP (classic) | rs356186 |
ClinGen | rs356186 |
ebi | rs356186 |
HLI | rs356186 |
Exac | rs356186 |
Gnomad | rs356186 |
Varsome | rs356186 |
LitVar | rs356186 |
Map | rs356186 |
PheGenI | rs356186 |
Biobank | rs356186 |
1000 genomes | rs356186 |
hgdp | rs356186 |
ensembl | rs356186 |
geneview | rs356186 |
scholar | rs356186 |
rs356186 | |
pharmgkb | rs356186 |
gwascentral | rs356186 |
openSNP | rs356186 |
23andMe | rs356186 |
SNPshot | rs356186 |
SNPdbe | rs356186 |
MSV3d | rs356186 |
GWAS Ctlg | rs356186 |
GMAF | 0.1703 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22104010] SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population
[PMID 15637659] Linkage disequilibrium patterns and tagSNP transferability among European populations.
[PMID 19771175] Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.
[PMID 25656566] Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: A meta-analysis
[PMID 30410434] A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease.