rs681591
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs681591(C;C) |
Make rs681591(C;T) |
Make rs681591(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 145832582 |
Gene | PRELID2 |
is a | snp |
is | mentioned by |
dbSNP | rs681591 |
dbSNP (classic) | rs681591 |
ClinGen | rs681591 |
ebi | rs681591 |
HLI | rs681591 |
Exac | rs681591 |
Gnomad | rs681591 |
Varsome | rs681591 |
LitVar | rs681591 |
Map | rs681591 |
PheGenI | rs681591 |
Biobank | rs681591 |
1000 genomes | rs681591 |
hgdp | rs681591 |
ensembl | rs681591 |
geneview | rs681591 |
scholar | rs681591 |
rs681591 | |
pharmgkb | rs681591 |
gwascentral | rs681591 |
openSNP | rs681591 |
23andMe | rs681591 |
SNPshot | rs681591 |
SNPdbe | rs681591 |
MSV3d | rs681591 |
GWAS Ctlg | rs681591 |
GMAF | 0.4302 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20937954] Mapping of Autosomal Dominant Cerebellar Ataxia Without the Pathogenic PPP2R2B Mutation to the Locus for Spinocerebellar Ataxia 12