rs1387389
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1387389(C;C) |
Make rs1387389(C;T) |
Make rs1387389(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 164720525 |
Gene | PBX1 |
is a | snp |
is | mentioned by |
dbSNP | rs1387389 |
dbSNP (classic) | rs1387389 |
ClinGen | rs1387389 |
ebi | rs1387389 |
HLI | rs1387389 |
Exac | rs1387389 |
Gnomad | rs1387389 |
Varsome | rs1387389 |
LitVar | rs1387389 |
Map | rs1387389 |
PheGenI | rs1387389 |
Biobank | rs1387389 |
1000 genomes | rs1387389 |
hgdp | rs1387389 |
ensembl | rs1387389 |
geneview | rs1387389 |
scholar | rs1387389 |
rs1387389 | |
pharmgkb | rs1387389 |
gwascentral | rs1387389 |
openSNP | rs1387389 |
23andMe | rs1387389 |
SNPshot | rs1387389 |
SNPdbe | rs1387389 |
MSV3d | rs1387389 |
GWAS Ctlg | rs1387389 |
GMAF | 0.3907 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23319801] |
Trait | Breast cancer (prognosis) |
Title | Identification of Inherited Genetic Variations Influencing Prognosis in Early-Onset Breast Cancer. |
Risk Allele | |
P-val | 4E-6 |
Odds Ratio | 1.28 [1.16-1.43] |