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rs2304973

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2304973(C;T)
Make rs2304973(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position4738927
GeneCXCL16, ZMYND15
is asnp
is mentioned by
dbSNPrs2304973
ebirs2304973
HLIrs2304973
Exacrs2304973
Varsomers2304973
Maprs2304973
PheGenIrs2304973
hapmaprs2304973
1000 genomesrs2304973
hgdprs2304973
ensemblrs2304973
gopubmedrs2304973
geneviewrs2304973
scholarrs2304973
googlers2304973
pharmgkbrs2304973
gwascentralrs2304973
openSNPrs2304973
23andMers2304973
23andMe allrs2304973
SNP Nexus

SNPshotrs2304973
SNPdbers2304973
MSV3drs2304973
GWAS Ctlgrs2304973
GMAF0.07805
Max Magnitude0
? (C;C) (C;T) (T;T) 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