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rs17369571

From SNPedia

Orientationplus
Stabilizedplus
Make rs17369571(A;A)
Make rs17369571(A;G)
Make rs17369571(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position21913486
is asnp
is mentioned by
dbSNPrs17369571
ebirs17369571
HLIrs17369571
Exacrs17369571
Varsomers17369571
Maprs17369571
PheGenIrs17369571
hapmaprs17369571
1000 genomesrs17369571
hgdprs17369571
ensemblrs17369571
gopubmedrs17369571
geneviewrs17369571
scholarrs17369571
googlers17369571
pharmgkbrs17369571
gwascentralrs17369571
openSNPrs17369571
23andMers17369571
23andMe allrs17369571
SNP Nexus

SNPshotrs17369571
SNPdbers17369571
MSV3drs17369571
GWAS Ctlgrs17369571
GMAF0.1309
Max Magnitude
? (A;A) (A;G) (G;G) 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 9.9999999999999995E-8
Odds Ratio NR NR

[PMID 18464913OA-icon.png] IL1RA / IL-1RA (IL1RN) protein levels


GET Evidence
rs17369571
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary