rs266085
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs266085(C;C) |
Make rs266085(C;T) |
Make rs266085(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 44378805 |
Gene | CXCL12 |
is a | snp |
is | mentioned by |
dbSNP | rs266085 |
dbSNP (classic) | rs266085 |
ClinGen | rs266085 |
ebi | rs266085 |
HLI | rs266085 |
Exac | rs266085 |
Gnomad | rs266085 |
Varsome | rs266085 |
LitVar | rs266085 |
Map | rs266085 |
PheGenI | rs266085 |
Biobank | rs266085 |
1000 genomes | rs266085 |
hgdp | rs266085 |
ensembl | rs266085 |
geneview | rs266085 |
scholar | rs266085 |
rs266085 | |
pharmgkb | rs266085 |
gwascentral | rs266085 |
openSNP | rs266085 |
23andMe | rs266085 |
SNPshot | rs266085 |
SNPdbe | rs266085 |
MSV3d | rs266085 |
GWAS Ctlg | rs266085 |
GMAF | 0.4013 |
Max Magnitude | 0 |
[PMID 19788587] Genetic variation in CXCL12 and risk of cervical carcinoma: a population-based case-control study
[PMID 19115008] SDF1 gene variation is associated with circulating SDF1alpha level and endothelial progenitor cell number: the Bruneck Study.
[PMID 23078136] Stromal-derived factor-1 gene variations in pediatric patients with primary immune thrombocytopenia
[PMID 26191295] CXCL12 rs266085 and TNF-α rs1799724 polymorphisms and susceptibility to cervical cancer in a Chinese population