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