rs12159200
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12159200(A;A) |
Make rs12159200(A;C) |
Make rs12159200(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 40646087 |
is a | snp |
is | mentioned by |
dbSNP | rs12159200 |
dbSNP (classic) | rs12159200 |
ClinGen | rs12159200 |
ebi | rs12159200 |
HLI | rs12159200 |
Exac | rs12159200 |
Gnomad | rs12159200 |
Varsome | rs12159200 |
LitVar | rs12159200 |
Map | rs12159200 |
PheGenI | rs12159200 |
Biobank | rs12159200 |
1000 genomes | rs12159200 |
hgdp | rs12159200 |
ensembl | rs12159200 |
geneview | rs12159200 |
scholar | rs12159200 |
rs12159200 | |
pharmgkb | rs12159200 |
gwascentral | rs12159200 |
openSNP | rs12159200 |
23andMe | rs12159200 |
SNPshot | rs12159200 |
SNPdbe | rs12159200 |
MSV3d | rs12159200 |
GWAS Ctlg | rs12159200 |
GMAF | 0.2658 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 6E-7 |
Odds Ratio | None None |