rs1460163
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1460163(A;A) |
Make rs1460163(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 79315213 |
is a | snp |
is | mentioned by |
dbSNP | rs1460163 |
dbSNP (classic) | rs1460163 |
ClinGen | rs1460163 |
ebi | rs1460163 |
HLI | rs1460163 |
Exac | rs1460163 |
Gnomad | rs1460163 |
Varsome | rs1460163 |
LitVar | rs1460163 |
Map | rs1460163 |
PheGenI | rs1460163 |
Biobank | rs1460163 |
1000 genomes | rs1460163 |
hgdp | rs1460163 |
ensembl | rs1460163 |
geneview | rs1460163 |
scholar | rs1460163 |
rs1460163 | |
pharmgkb | rs1460163 |
gwascentral | rs1460163 |
openSNP | rs1460163 |
23andMe | rs1460163 |
SNPshot | rs1460163 |
SNPdbe | rs1460163 |
MSV3d | rs1460163 |
GWAS Ctlg | rs1460163 |
GMAF | 0.2466 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19081515] |
Trait | Creutzfeldt-Jakob disease |
Title | Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study |
Risk Allele | A |
P-val | 6E-8 |
Odds Ratio | NR NR |