rs17763373
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 |
Make rs17763373(A;G) |
Make rs17763373(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 173932328 |
Gene | CPEB4 |
is a | snp |
is | mentioned by |
dbSNP | rs17763373 |
dbSNP (classic) | rs17763373 |
ClinGen | rs17763373 |
ebi | rs17763373 |
HLI | rs17763373 |
Exac | rs17763373 |
Gnomad | rs17763373 |
Varsome | rs17763373 |
LitVar | rs17763373 |
Map | rs17763373 |
PheGenI | rs17763373 |
Biobank | rs17763373 |
1000 genomes | rs17763373 |
hgdp | rs17763373 |
ensembl | rs17763373 |
geneview | rs17763373 |
scholar | rs17763373 |
rs17763373 | |
pharmgkb | rs17763373 |
gwascentral | rs17763373 |
openSNP | rs17763373 |
23andMe | rs17763373 |
SNPshot | rs17763373 |
SNPdbe | rs17763373 |
MSV3d | rs17763373 |
GWAS Ctlg | rs17763373 |
GMAF | 0.03168 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22210626![]() |
Trait | |
Title | Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | 1.5106 None |