rs2304973

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs2304973(C;T)

Make rs2304973(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

4738927

Gene	CXCL16, ZMYND15

is a	snp
is	mentioned by
dbSNP	rs2304973
dbSNP (classic)	rs2304973
ClinGen	rs2304973
ebi	rs2304973
HLI	rs2304973
Exac	rs2304973
Gnomad	rs2304973
Varsome	rs2304973
LitVar	rs2304973
Map	rs2304973
PheGenI	rs2304973
Biobank	rs2304973
1000 genomes	rs2304973
hgdp	rs2304973
ensembl	rs2304973
geneview	rs2304973
scholar	rs2304973
google	rs2304973
pharmgkb	rs2304973
gwascentral	rs2304973
openSNP	rs2304973
23andMe	rs2304973
SNPshot	rs2304973
SNPdbe	rs2304973
MSV3d	rs2304973
GWAS Ctlg	rs2304973

GMAF

0.07805

Max Magnitude

0

?

(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