rs16858811

Orientation

minus

Stabilized

minus

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

Make rs16858811(G;G)

Make rs16858811(G;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

218165120

Gene

CXCR1

is a	snp
is	mentioned by
dbSNP	rs16858811
dbSNP (classic)	rs16858811
ClinGen	rs16858811
ebi	rs16858811
HLI	rs16858811
Exac	rs16858811
Gnomad	rs16858811
Varsome	rs16858811
LitVar	rs16858811
Map	rs16858811
PheGenI	rs16858811
Biobank	rs16858811
1000 genomes	rs16858811
hgdp	rs16858811
ensembl	rs16858811
geneview	rs16858811
scholar	rs16858811
google	rs16858811
pharmgkb	rs16858811
gwascentral	rs16858811
openSNP	rs16858811
23andMe	rs16858811
SNPshot	rs16858811
SNPdbe	rs16858811
MSV3d	rs16858811
GWAS Ctlg	rs16858811

GMAF

0.03673

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

OMIM	609423
Desc	HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
Variant
Related	also

OMIM	146929
Desc	INTERLEUKIN 8 RECEPTOR, ALPHA; IL8RA
Variant
Related	also

OMIM	146929
Desc
Variant	0001
Related	also

[PMID 16503988] Impact of IL8 and IL8-receptor alpha polymorphisms on the genetics of bronchial asthma and severe RSV infections.

[PMID 17360650] A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients.

[PMID 20016852] Genetic variation of the human urinary tract innate immune response and asymptomatic bacteriuria in women.