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rs377584435

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377584435(C;T)
Make rs377584435(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position43768145
GeneIRAK4
is asnp
is mentioned by
dbSNPrs377584435
ebirs377584435
HLIrs377584435
Exacrs377584435
Varsomers377584435
Maprs377584435
PheGenIrs377584435
hapmaprs377584435
1000 genomesrs377584435
hgdprs377584435
ensemblrs377584435
gopubmedrs377584435
geneviewrs377584435
scholarrs377584435
googlers377584435
pharmgkbrs377584435
gwascentralrs377584435
openSNPrs377584435
23andMers377584435
23andMe allrs377584435
SNP Nexus

SNPshotrs377584435
SNPdbers377584435
MSV3drs377584435
GWAS Ctlgrs377584435
Max Magnitude0
ClinVar
Risk rs377584435(T;T)
Alt rs377584435(T;T)
Reference rs377584435(C;C)
Significance Pathogenic
Disease IRAK4 deficiency
Variation info
Gene IRAK4
CLNDBN IRAK4 deficiency
Reversed 0
HGVS NC_000012.11:g.44161948C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023583.2,