rs3744700
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Make rs3744700(G;G) | 
| Make rs3744700(G;T) | 
| Make rs3744700(T;T) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 17 | 
| Position | 4734715 | 
| Gene | CXCL16 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs3744700 | 
| dbSNP (classic) | rs3744700 | 
| ClinGen | rs3744700 | 
| ebi | rs3744700 | 
| HLI | rs3744700 | 
| Exac | rs3744700 | 
| Gnomad | rs3744700 | 
| Varsome | rs3744700 | 
| LitVar | rs3744700 | 
| Map | rs3744700 | 
| PheGenI | rs3744700 | 
| Biobank | rs3744700 | 
| 1000 genomes | rs3744700 | 
| hgdp | rs3744700 | 
| ensembl | rs3744700 | 
| geneview | rs3744700 | 
| scholar | rs3744700 | 
| rs3744700 | |
| pharmgkb | rs3744700 | 
| gwascentral | rs3744700 | 
| openSNP | rs3744700 | 
| 23andMe | rs3744700 | 
| SNPshot | rs3744700 | 
| SNPdbe | rs3744700 | 
| MSV3d | rs3744700 | 
| GWAS Ctlg | rs3744700 | 
| GMAF | 0.2851 | 
| Max Magnitude | 0 | 
| ? | (G;G) (G;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
Categories: 
- Is a snp
 - In dbSNP
 - SNPs on chromosome 17
 - Has genotype
 - Has population
 - On chip 23andMe v1
 - On chip 23andMe v2
 - On chip 23andMe v3
 - On chip 23andMe v4
 - On chip Affy GenomeWide 6
 - On chip Ancestry v2
 - On chip FTDNA2
 - On chip FTDNA
 - On chip HumanOmni1Quad
 - On chip Illumina Human 1M
 - On chip 23andMe v5
 - On chip Ancestry v2c
 - On chip Ancestry v2d
 
