rs2076600
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2076600(C;C) |
Make rs2076600(C;T) |
Make rs2076600(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 17010896 |
Gene | ATP13A2 |
is a | snp |
is | mentioned by |
dbSNP | rs2076600 |
dbSNP (classic) | rs2076600 |
ClinGen | rs2076600 |
ebi | rs2076600 |
HLI | rs2076600 |
Exac | rs2076600 |
Gnomad | rs2076600 |
Varsome | rs2076600 |
LitVar | rs2076600 |
Map | rs2076600 |
PheGenI | rs2076600 |
Biobank | rs2076600 |
1000 genomes | rs2076600 |
hgdp | rs2076600 |
ensembl | rs2076600 |
geneview | rs2076600 |
scholar | rs2076600 |
rs2076600 | |
pharmgkb | rs2076600 |
gwascentral | rs2076600 |
openSNP | rs2076600 |
23andMe | rs2076600 |
SNPshot | rs2076600 |
SNPdbe | rs2076600 |
MSV3d | rs2076600 |
GWAS Ctlg | rs2076600 |
GMAF | 0.3875 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22285144] ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese