rs1829975
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1829975(A;A) |
Make rs1829975(A;G) |
Make rs1829975(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 160928658 |
is a | snp |
is | mentioned by |
dbSNP | rs1829975 |
dbSNP (classic) | rs1829975 |
ClinGen | rs1829975 |
ebi | rs1829975 |
HLI | rs1829975 |
Exac | rs1829975 |
Gnomad | rs1829975 |
Varsome | rs1829975 |
LitVar | rs1829975 |
Map | rs1829975 |
PheGenI | rs1829975 |
Biobank | rs1829975 |
1000 genomes | rs1829975 |
hgdp | rs1829975 |
ensembl | rs1829975 |
geneview | rs1829975 |
scholar | rs1829975 |
rs1829975 | |
pharmgkb | rs1829975 |
gwascentral | rs1829975 |
openSNP | rs1829975 |
23andMe | rs1829975 |
SNPshot | rs1829975 |
SNPdbe | rs1829975 |
MSV3d | rs1829975 |
GWAS Ctlg | rs1829975 |
GMAF | 0.2277 |
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 | 0.000006 |
Odds Ratio | None None |