rs1858973
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1858973(A;A) |
Make rs1858973(A;G) |
Make rs1858973(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 19732327 |
Gene | IQCK |
is a | snp |
is | mentioned by |
dbSNP | rs1858973 |
dbSNP (classic) | rs1858973 |
ClinGen | rs1858973 |
ebi | rs1858973 |
HLI | rs1858973 |
Exac | rs1858973 |
Gnomad | rs1858973 |
Varsome | rs1858973 |
LitVar | rs1858973 |
Map | rs1858973 |
PheGenI | rs1858973 |
Biobank | rs1858973 |
1000 genomes | rs1858973 |
hgdp | rs1858973 |
ensembl | rs1858973 |
geneview | rs1858973 |
scholar | rs1858973 |
rs1858973 | |
pharmgkb | rs1858973 |
gwascentral | rs1858973 |
openSNP | rs1858973 |
23andMe | rs1858973 |
SNPshot | rs1858973 |
SNPdbe | rs1858973 |
MSV3d | rs1858973 |
GWAS Ctlg | rs1858973 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24788522] Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity