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rs2277680

From SNPedia

Orientationplus
Stabilizedplus
Make rs2277680(A;A)
Make rs2277680(A;G)
Make rs2277680(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position4735268
GeneCXCL16
is asnp
is mentioned by
dbSNPrs2277680
ebirs2277680
HLIrs2277680
Exacrs2277680
Varsomers2277680
Maprs2277680
PheGenIrs2277680
hapmaprs2277680
1000 genomesrs2277680
hgdprs2277680
ensemblrs2277680
gopubmedrs2277680
geneviewrs2277680
scholarrs2277680
googlers2277680
pharmgkbrs2277680
gwascentralrs2277680
openSNPrs2277680
23andMers2277680
23andMe allrs2277680
SNP Nexus

SNPshotrs2277680
SNPdbers2277680
MSV3drs2277680
GWAS Ctlgrs2277680
GMAF0.4518
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19954776] An intron polymorphism in the CXCL16 gene is associated with increased risk of coronary artery disease in Chinese Han population: A large angiography-based study


[PMID 17848170OA-icon.png] The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.


GET Evidence
CXCL16-A200V
aa_change Ala200Val
aa_change_short A200V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.39775
summary



[PMID 27069792] Association of NOD1, CXCL16, STAT6 and TLR4 gene polymorphisms with Malaysian patients with Crohn's disease