rs32582
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs32582(G;G) |
Make rs32582(G;T) |
Make rs32582(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 149825854 |
Gene | PPARGC1B |
is a | snp |
is | mentioned by |
dbSNP | rs32582 |
dbSNP (classic) | rs32582 |
ClinGen | rs32582 |
ebi | rs32582 |
HLI | rs32582 |
Exac | rs32582 |
Gnomad | rs32582 |
Varsome | rs32582 |
LitVar | rs32582 |
Map | rs32582 |
PheGenI | rs32582 |
Biobank | rs32582 |
1000 genomes | rs32582 |
hgdp | rs32582 |
ensembl | rs32582 |
geneview | rs32582 |
scholar | rs32582 |
rs32582 | |
pharmgkb | rs32582 |
gwascentral | rs32582 |
openSNP | rs32582 |
23andMe | rs32582 |
SNPshot | rs32582 |
SNPdbe | rs32582 |
MSV3d | rs32582 |
GWAS Ctlg | rs32582 |
GMAF | 0.2057 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 20937954] Mapping of Autosomal Dominant Cerebellar Ataxia Without the Pathogenic PPP2R2B Mutation to the Locus for Spinocerebellar Ataxia 12