rs2871776
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2871776(A;A) |
Make rs2871776(A;G) |
Make rs2871776(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 17001806 |
Gene | ATP13A2 |
is a | snp |
is | mentioned by |
dbSNP | rs2871776 |
dbSNP (classic) | rs2871776 |
ClinGen | rs2871776 |
ebi | rs2871776 |
HLI | rs2871776 |
Exac | rs2871776 |
Gnomad | rs2871776 |
Varsome | rs2871776 |
LitVar | rs2871776 |
Map | rs2871776 |
PheGenI | rs2871776 |
Biobank | rs2871776 |
1000 genomes | rs2871776 |
hgdp | rs2871776 |
ensembl | rs2871776 |
geneview | rs2871776 |
scholar | rs2871776 |
rs2871776 | |
pharmgkb | rs2871776 |
gwascentral | rs2871776 |
openSNP | rs2871776 |
23andMe | rs2871776 |
SNPshot | rs2871776 |
SNPdbe | rs2871776 |
MSV3d | rs2871776 |
GWAS Ctlg | rs2871776 |
GMAF | 0.3884 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22285144] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese