rs1915279
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1915279(A;A) |
Make rs1915279(A;G) |
Make rs1915279(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 238912414 |
is a | snp |
is | mentioned by |
dbSNP | rs1915279 |
dbSNP (classic) | rs1915279 |
ClinGen | rs1915279 |
ebi | rs1915279 |
HLI | rs1915279 |
Exac | rs1915279 |
Gnomad | rs1915279 |
Varsome | rs1915279 |
LitVar | rs1915279 |
Map | rs1915279 |
PheGenI | rs1915279 |
Biobank | rs1915279 |
1000 genomes | rs1915279 |
hgdp | rs1915279 |
ensembl | rs1915279 |
geneview | rs1915279 |
scholar | rs1915279 |
rs1915279 | |
pharmgkb | rs1915279 |
gwascentral | rs1915279 |
openSNP | rs1915279 |
23andMe | rs1915279 |
SNPshot | rs1915279 |
SNPdbe | rs1915279 |
MSV3d | rs1915279 |
GWAS Ctlg | rs1915279 |
GMAF | 0.3182 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22310353] |
Trait | |
Title | Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis. |
Risk Allele | |
P-val | 0.000002 |
Odds Ratio | None None |