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rs266093

From SNPedia

Orientationplus
Stabilizedplus
Make rs266093(C;C)
Make rs266093(C;G)
Make rs266093(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position44370760
GeneCXCL12
is asnp
is mentioned by
dbSNPrs266093
ClinGenrs266093
ebirs266093
HLIrs266093
Exacrs266093
Varsomers266093
Maprs266093
PheGenIrs266093
hapmaprs266093
1000 genomesrs266093
hgdprs266093
ensemblrs266093
gopubmedrs266093
geneviewrs266093
scholarrs266093
googlers266093
pharmgkbrs266093
gwascentralrs266093
openSNPrs266093
23andMers266093
23andMe allrs266093
SNP Nexus

SNPshotrs266093
SNPdbers266093
MSV3drs266093
GWAS Ctlgrs266093
GMAF0.3251
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19788587OA-icon.png] Genetic variation in CXCL12 and risk of cervical carcinoma: a population-based case-control study


[PMID 19956101OA-icon.png] Overview of the Rapid Response data.


[PMID 21296802] Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women.