Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853064
rs137853064
MYD88
0.800 GeneticVariation UNIPROT Functional assessment of the mutational effects of human IRAK4 and MyD88 genes. 24316379

2014
dbSNP: rs137853065
rs137853065
ACAA1 ; MYD88
0.800 GeneticVariation UNIPROT Functional assessment of the mutational effects of human IRAK4 and MyD88 genes. 24316379

2014
dbSNP: rs137853064
rs137853064
MYD88
0.800 GeneticVariation UNIPROT Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency. 21057262

2010
dbSNP: rs137853065
rs137853065
ACAA1 ; MYD88
0.800 GeneticVariation UNIPROT Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency. 21057262

2010
dbSNP: rs137853064
rs137853064
MYD88
0.800 GeneticVariation UNIPROT Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling. 19506249

2009
dbSNP: rs137853065
rs137853065
ACAA1 ; MYD88
0.800 GeneticVariation UNIPROT Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling. 19506249

2009
dbSNP: rs137853064
rs137853064
MYD88
0.800 GeneticVariation UNIPROT Pyogenic bacterial infections in humans with MyD88 deficiency. 18669862

2008
dbSNP: rs137853065
rs137853065
ACAA1 ; MYD88
0.800 GeneticVariation UNIPROT Pyogenic bacterial infections in humans with MyD88 deficiency. 18669862

2008
dbSNP: rs137853064
rs137853064
MYD88
T 0.800 CausalMutation CLINVAR

dbSNP: rs137853065
rs137853065
ACAA1 ; MYD88
C 0.800 CausalMutation CLINVAR

dbSNP: rs746651350
rs746651350
ACAA1 ; MYD88
C 0.700 CausalMutation CLINVAR

dbSNP: rs878852993
rs878852993
ACAA1 ; MYD88
C 0.700 CausalMutation CLINVAR