rs8126696
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8126696(C;C) |
Make rs8126696(C;T) |
Make rs8126696(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 37358422 |
is a | snp |
is | mentioned by |
dbSNP | rs8126696 |
dbSNP (classic) | rs8126696 |
ClinGen | rs8126696 |
ebi | rs8126696 |
HLI | rs8126696 |
Exac | rs8126696 |
Gnomad | rs8126696 |
Varsome | rs8126696 |
LitVar | rs8126696 |
Map | rs8126696 |
PheGenI | rs8126696 |
Biobank | rs8126696 |
1000 genomes | rs8126696 |
hgdp | rs8126696 |
ensembl | rs8126696 |
geneview | rs8126696 |
scholar | rs8126696 |
rs8126696 | |
pharmgkb | rs8126696 |
gwascentral | rs8126696 |
openSNP | rs8126696 |
23andMe | rs8126696 |
SNPshot | rs8126696 |
SNPdbe | rs8126696 |
MSV3d | rs8126696 |
GWAS Ctlg | rs8126696 |
GMAF | 0.4086 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22269890] A Pilot Study Examining Associations between DYRK1A and ?-Synuclein Dementias
[PMID 19995442] DYRK1A genetic variants are not linked to Alzheimer's disease in a Spanish case-control cohort.
[PMID 27546826] Association of DYRK1A polymorphisms with sporadic Parkinson's disease in Chinese Han population.