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rs10191411

From SNPedia

Orientationplus
Stabilizedplus
Make rs10191411(C;C)
Make rs10191411(C;T)
Make rs10191411(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position148630399
is asnp
is mentioned by
dbSNPrs10191411
ebirs10191411
HLIrs10191411
Exacrs10191411
Varsomers10191411
Maprs10191411
PheGenIrs10191411
hapmaprs10191411
1000 genomesrs10191411
hgdprs10191411
ensemblrs10191411
gopubmedrs10191411
geneviewrs10191411
scholarrs10191411
googlers10191411
pharmgkbrs10191411
gwascentralrs10191411
openSNPrs10191411
23andMers10191411
23andMe allrs10191411
SNP Nexus

SNPshotrs10191411
SNPdbers10191411
MSV3drs10191411
GWAS Ctlgrs10191411
GMAF0.4343
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 0.0000039999999999999998
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Interleukin 8 (IL8) protein levels


GET Evidence
rs10191411
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445312
summary