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rs2228014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs2228014(C;T)
Make rs2228014(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position136115514
GeneCXCR4
is asnp
is mentioned by
dbSNPrs2228014
dbSNP (classic)rs2228014
ClinGenrs2228014
ebirs2228014
HLIrs2228014
Exacrs2228014
Gnomadrs2228014
Varsomers2228014
LitVarrs2228014
Maprs2228014
PheGenIrs2228014
Biobankrs2228014
1000 genomesrs2228014
hgdprs2228014
ensemblrs2228014
geneviewrs2228014
scholarrs2228014
googlers2228014
pharmgkbrs2228014
gwascentralrs2228014
openSNPrs2228014
23andMers2228014
SNPshotrs2228014
SNPdbers2228014
MSV3drs2228014
GWAS Ctlgrs2228014
GMAF0.05969
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 21292343] the TT genotype increased 6.5X risk of lung cancer compared with CC genotype in chinese.


[PMID 18781190OA-icon.png] Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study).


[PMID 19196101] Combinational polymorphisms of seven CXCL12-related genes are protective against breast cancer in Taiwan.


[PMID 19327121] Stromal cell-derived factor-1 but not its receptor, CXCR4, gene variants increase susceptibility and pathological development of hepatocellular carcinoma.


[PMID 19812382] Genetic variation in CXCR4 and risk of chronic lymphocytic leukemia.


[PMID 21304904OA-icon.png] Genetic predisposition of donors affects the allograft outcome in kidney transplantation; polymorphisms of stromal-derived factor-1 and CXC receptor 4.


[PMID 23711392] The CXCL12-3'A allele plays a favourable role in patients with multiple myeloma


[PMID 27200368OA-icon.png] Genetic Variants of CD40 Gene Are Associated with Coronary Artery Disease and Blood Lipid Levels.


ClinVar
Risk rs2228014(T;T)
Alt rs2228014(T;T)
Reference Rs2228014(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CXCR4
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.136873084G>A
CLNSRC
CLNACC RCV000254216.1,