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rs8126696

From SNPedia

Orientationplus
Stabilizedplus
Make rs8126696(C;C)
Make rs8126696(C;T)
Make rs8126696(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position37358422
is asnp
is mentioned by
dbSNPrs8126696
dbSNP (classic)rs8126696
ClinGenrs8126696
ebirs8126696
HLIrs8126696
Exacrs8126696
Gnomadrs8126696
Varsomers8126696
LitVarrs8126696
Maprs8126696
PheGenIrs8126696
Biobankrs8126696
1000 genomesrs8126696
hgdprs8126696
ensemblrs8126696
geneviewrs8126696
scholarrs8126696
googlers8126696
pharmgkbrs8126696
gwascentralrs8126696
openSNPrs8126696
23andMers8126696
SNPshotrs8126696
SNPdbers8126696
MSV3drs8126696
GWAS Ctlgrs8126696
GMAF0.4086
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22269890] A Pilot Study Examining Associations between DYRK1A and ?-Synuclein Dementias


[PMID 19995442OA-icon.png] 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.