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rs266085

From SNPedia

Orientationplus
Stabilizedplus
Make rs266085(C;C)
Make rs266085(C;T)
Make rs266085(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position44378805
GeneCXCL12
is asnp
is mentioned by
dbSNPrs266085
ebirs266085
HLIrs266085
Exacrs266085
Varsomers266085
Maprs266085
PheGenIrs266085
hapmaprs266085
1000 genomesrs266085
hgdprs266085
ensemblrs266085
gopubmedrs266085
geneviewrs266085
scholarrs266085
googlers266085
pharmgkbrs266085
gwascentralrs266085
openSNPrs266085
23andMers266085
23andMe allrs266085
SNP Nexus

SNPshotrs266085
SNPdbers266085
MSV3drs266085
GWAS Ctlgrs266085
GMAF0.4013
Max Magnitude

[PMID 19788587OA-icon.png] Genetic variation in CXCL12 and risk of cervical carcinoma: a population-based case-control study


[PMID 19115008OA-icon.png] 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 26191295OA-icon.png] CXCL12 rs266085 and TNF-α rs1799724 polymorphisms and susceptibility to cervical cancer in a Chinese population