rs12456492
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12456492(A;A) |
Make rs12456492(A;G) |
Make rs12456492(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 43093415 |
Gene | RIT2 |
is a | snp |
is | mentioned by |
dbSNP | rs12456492 |
dbSNP (classic) | rs12456492 |
ClinGen | rs12456492 |
ebi | rs12456492 |
HLI | rs12456492 |
Exac | rs12456492 |
Gnomad | rs12456492 |
Varsome | rs12456492 |
LitVar | rs12456492 |
Map | rs12456492 |
PheGenI | rs12456492 |
Biobank | rs12456492 |
1000 genomes | rs12456492 |
hgdp | rs12456492 |
ensembl | rs12456492 |
geneview | rs12456492 |
scholar | rs12456492 |
rs12456492 | |
pharmgkb | rs12456492 |
gwascentral | rs12456492 |
openSNP | rs12456492 |
23andMe | rs12456492 |
SNPshot | rs12456492 |
SNPdbe | rs12456492 |
MSV3d | rs12456492 |
GWAS Ctlg | rs12456492 |
GMAF | 0.3384 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22451204] Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2
[PMID 26188085] RIT2 rs12456492 polymorphism and the risk of Parkinson's disease: A meta-analysis