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rs1141168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1141168(A;G)
Make rs1141168(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position43788903
GeneIRAK4
is asnp
is mentioned by
dbSNPrs1141168
dbSNP (old)rs1141168
ClinGenrs1141168
ebirs1141168
HLIrs1141168
Exacrs1141168
Gnomadrs1141168
Varsomers1141168
Maprs1141168
PheGenIrs1141168
Biobankrs1141168
1000 genomesrs1141168
hgdprs1141168
ensemblrs1141168
gopubmedrs1141168
geneviewrs1141168
scholarrs1141168
googlers1141168
pharmgkbrs1141168
gwascentralrs1141168
openSNPrs1141168
23andMers1141168
23andMe allrs1141168
SNP Nexus

SNPshotrs1141168
SNPdbers1141168
MSV3drs1141168
GWAS Ctlgrs1141168
Merged fromRs4251559
GMAF0.421
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 19254290] Polymorphisms in interleukin-1 receptor-associated kinase 4 are associated with total serum IgE.


[PMID 19505919OA-icon.png] Toll-like receptor signaling pathway variants and prostate cancer mortality.


ClinVar
Risk rs1141168(G;G)
Alt rs1141168(G;G)
Reference Rs1141168(A;A)
Significance Non-pathogenic
Disease IRAK4 deficiency
Variation info
Gene IRAK4
CLNDBN IRAK4 deficiency
Reversed 0
HGVS NC_000012.11:g.44182706A>G
CLNSRC
CLNACC RCV000395832.1,