rs1491942
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1491942(C;C) |
Make rs1491942(C;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 40227006 |
Gene | LRRK2 |
is a | snp |
is | mentioned by |
dbSNP | rs1491942 |
dbSNP (classic) | rs1491942 |
ClinGen | rs1491942 |
ebi | rs1491942 |
HLI | rs1491942 |
Exac | rs1491942 |
Gnomad | rs1491942 |
Varsome | rs1491942 |
LitVar | rs1491942 |
Map | rs1491942 |
PheGenI | rs1491942 |
Biobank | rs1491942 |
1000 genomes | rs1491942 |
hgdp | rs1491942 |
ensembl | rs1491942 |
geneview | rs1491942 |
scholar | rs1491942 |
rs1491942 | |
pharmgkb | rs1491942 |
gwascentral | rs1491942 |
openSNP | rs1491942 |
23andMe | rs1491942 |
SNPshot | rs1491942 |
SNPdbe | rs1491942 |
MSV3d | rs1491942 |
GWAS Ctlg | rs1491942 |
GMAF | 0.2741 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
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 | 6E-14 |
Odds Ratio | 1.2700 [1.21-1.33] |
GWAS snp | |
---|---|
PMID | [PMID 22438815] |
Trait | |
Title | Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. |
Risk Allele | |
P-val | 6E-15 |
Odds Ratio | 1.1700 None |
[PMID 33574311] Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry.