Have questions? Visit https://www.reddit.com/r/SNPedia

rs7626795

From SNPedia

Orientationplus
Stabilizedplus
Make rs7626795(A;A)
Make rs7626795(A;G)
Make rs7626795(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position190632672
GeneIL1RAP
is asnp
is mentioned by
dbSNPrs7626795
ebirs7626795
HLIrs7626795
Exacrs7626795
Varsomers7626795
Maprs7626795
PheGenIrs7626795
hapmaprs7626795
1000 genomesrs7626795
hgdprs7626795
ensemblrs7626795
gopubmedrs7626795
geneviewrs7626795
scholarrs7626795
googlers7626795
pharmgkbrs7626795
gwascentralrs7626795
openSNPrs7626795
23andMers7626795
23andMe allrs7626795
SNP Nexus

SNPshotrs7626795
SNPdbers7626795
MSV3drs7626795
GWAS Ctlgrs7626795
GMAF0.2401
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs7626795
PubMedID [PMID 18385676OA-icon.png]
Condition Lung cancer
Gene IL1RAP
Risk Allele G
pValue 8.00E-006
OR 1.16
95% CI 1.05-1.28



[PMID 19468064OA-icon.png] Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.


[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.


GET Evidence
rs7626795
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.21875
summary