rs1559085
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 |
Make rs1559085(C;C) |
Make rs1559085(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 96742998 |
Gene | CAST |
is a | snp |
is | mentioned by |
dbSNP | rs1559085 |
dbSNP (classic) | rs1559085 |
ClinGen | rs1559085 |
ebi | rs1559085 |
HLI | rs1559085 |
Exac | rs1559085 |
Gnomad | rs1559085 |
Varsome | rs1559085 |
LitVar | rs1559085 |
Map | rs1559085 |
PheGenI | rs1559085 |
Biobank | rs1559085 |
1000 genomes | rs1559085 |
hgdp | rs1559085 |
ensembl | rs1559085 |
geneview | rs1559085 |
scholar | rs1559085 |
rs1559085 | |
pharmgkb | rs1559085 |
gwascentral | rs1559085 |
openSNP | rs1559085 |
23andMe | rs1559085 |
SNPshot | rs1559085 |
SNPdbe | rs1559085 |
MSV3d | rs1559085 |
GWAS Ctlg | rs1559085 |
GMAF | 0.06566 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs1559085 is a SNP in the calpastatin CAST gene.
A significant association (p = 0.0167) between Parkinson's disease and rs1559085 was found in an analysis of the Center for Inherited Disease Research's (CIDR) genome-wide association study in familial PD. [PMID 20127884]
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.