rs1168987
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1168987(A;A) |
Make rs1168987(A;G) |
Make rs1168987(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 14 |
Position | 35928474 |
is a | snp |
is | mentioned by |
dbSNP | rs1168987 |
dbSNP (classic) | rs1168987 |
ClinGen | rs1168987 |
ebi | rs1168987 |
HLI | rs1168987 |
Exac | rs1168987 |
Gnomad | rs1168987 |
Varsome | rs1168987 |
LitVar | rs1168987 |
Map | rs1168987 |
PheGenI | rs1168987 |
Biobank | rs1168987 |
1000 genomes | rs1168987 |
hgdp | rs1168987 |
ensembl | rs1168987 |
geneview | rs1168987 |
scholar | rs1168987 |
rs1168987 | |
pharmgkb | rs1168987 |
gwascentral | rs1168987 |
openSNP | rs1168987 |
23andMe | rs1168987 |
SNPshot | rs1168987 |
SNPdbe | rs1168987 |
MSV3d | rs1168987 |
GWAS Ctlg | rs1168987 |
GMAF | 0.1281 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21659360![]() |
Trait | |
Title | Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. |
Risk Allele | A |
P-val | 0.000005 |
Odds Ratio | 2.2700 [0.31-0.63] |