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rs16858811

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16858811(G;G)
Make rs16858811(G;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position218165120
GeneCXCR1
is asnp
is mentioned by
dbSNPrs16858811
ebirs16858811
HLIrs16858811
Exacrs16858811
Varsomers16858811
Maprs16858811
PheGenIrs16858811
hapmaprs16858811
1000 genomesrs16858811
hgdprs16858811
ensemblrs16858811
gopubmedrs16858811
geneviewrs16858811
scholarrs16858811
googlers16858811
pharmgkbrs16858811
gwascentralrs16858811
openSNPrs16858811
23andMers16858811
23andMe allrs16858811
SNP Nexus

SNPshotrs16858811
SNPdbers16858811
MSV3drs16858811
GWAS Ctlgrs16858811
GMAF0.03673
Max Magnitude0
? (G;G) (G;T) (T;T) 28
OMIM609423
DescHUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
Variant
Relatedalso
OMIM146929
DescINTERLEUKIN 8 RECEPTOR, ALPHA; IL8RA
Variant
Relatedalso
OMIM146929
Desc
Variant0001
Relatedalso
[PMID 16503988OA-icon.png] Impact of IL8 and IL8-receptor alpha polymorphisms on the genetics of bronchial asthma and severe RSV infections.


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


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


GET Evidence
CXCR1-M31R
aa_change Met31Arg
aa_change_short M31R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0403421
summary