rs295301
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs295301(A;A) |
Make rs295301(A;G) |
Make rs295301(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 141619799 |
is a | snp |
is | mentioned by |
dbSNP | rs295301 |
dbSNP (classic) | rs295301 |
ClinGen | rs295301 |
ebi | rs295301 |
HLI | rs295301 |
Exac | rs295301 |
Gnomad | rs295301 |
Varsome | rs295301 |
LitVar | rs295301 |
Map | rs295301 |
PheGenI | rs295301 |
Biobank | rs295301 |
1000 genomes | rs295301 |
hgdp | rs295301 |
ensembl | rs295301 |
geneview | rs295301 |
scholar | rs295301 |
rs295301 | |
pharmgkb | rs295301 |
gwascentral | rs295301 |
openSNP | rs295301 |
23andMe | rs295301 |
SNPshot | rs295301 |
SNPdbe | rs295301 |
MSV3d | rs295301 |
GWAS Ctlg | rs295301 |
GMAF | 0.3866 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22210626] Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP