rs2669858
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2669858(C;C) |
Make rs2669858(C;T) |
Make rs2669858(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 130946687 |
Gene | ATP2C1 |
is a | snp |
is | mentioned by |
dbSNP | rs2669858 |
dbSNP (classic) | rs2669858 |
ClinGen | rs2669858 |
ebi | rs2669858 |
HLI | rs2669858 |
Exac | rs2669858 |
Gnomad | rs2669858 |
Varsome | rs2669858 |
LitVar | rs2669858 |
Map | rs2669858 |
PheGenI | rs2669858 |
Biobank | rs2669858 |
1000 genomes | rs2669858 |
hgdp | rs2669858 |
ensembl | rs2669858 |
geneview | rs2669858 |
scholar | rs2669858 |
rs2669858 | |
pharmgkb | rs2669858 |
gwascentral | rs2669858 |
openSNP | rs2669858 |
23andMe | rs2669858 |
SNPshot | rs2669858 |
SNPdbe | rs2669858 |
MSV3d | rs2669858 |
GWAS Ctlg | rs2669858 |
GMAF | 0.1387 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22285144] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese