rs1022442
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1022442(A;A) |
Make rs1022442(A;G) |
Make rs1022442(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 20983528 |
is a | snp |
is | mentioned by |
dbSNP | rs1022442 |
dbSNP (classic) | rs1022442 |
ClinGen | rs1022442 |
ebi | rs1022442 |
HLI | rs1022442 |
Exac | rs1022442 |
Gnomad | rs1022442 |
Varsome | rs1022442 |
LitVar | rs1022442 |
Map | rs1022442 |
PheGenI | rs1022442 |
Biobank | rs1022442 |
1000 genomes | rs1022442 |
hgdp | rs1022442 |
ensembl | rs1022442 |
geneview | rs1022442 |
scholar | rs1022442 |
rs1022442 | |
pharmgkb | rs1022442 |
gwascentral | rs1022442 |
openSNP | rs1022442 |
23andMe | rs1022442 |
SNPshot | rs1022442 |
SNPdbe | rs1022442 |
MSV3d | rs1022442 |
GWAS Ctlg | rs1022442 |
GMAF | 0.3586 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20932310] Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study