rs2071598
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2071598(A;A) |
Make rs2071598(A;C) |
Make rs2071598(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 98117279 |
Gene | POP1, RIDA |
is a | snp |
is | mentioned by |
dbSNP | rs2071598 |
dbSNP (classic) | rs2071598 |
ClinGen | rs2071598 |
ebi | rs2071598 |
HLI | rs2071598 |
Exac | rs2071598 |
Gnomad | rs2071598 |
Varsome | rs2071598 |
LitVar | rs2071598 |
Map | rs2071598 |
PheGenI | rs2071598 |
Biobank | rs2071598 |
1000 genomes | rs2071598 |
hgdp | rs2071598 |
ensembl | rs2071598 |
geneview | rs2071598 |
scholar | rs2071598 |
rs2071598 | |
pharmgkb | rs2071598 |
gwascentral | rs2071598 |
openSNP | rs2071598 |
23andMe | rs2071598 |
SNPshot | rs2071598 |
SNPdbe | rs2071598 |
MSV3d | rs2071598 |
GWAS Ctlg | rs2071598 |
GMAF | 0.1869 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 0.000009 |
Odds Ratio | 1.2646 None |