Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893674
rs104893674
0.700 GeneticVariation UNIPROT Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency. 18509675

2009

dbSNP: rs137853201
rs137853201
0.700 GeneticVariation UNIPROT Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency. 18509675

2009

dbSNP: rs104893674
rs104893674
0.700 GeneticVariation UNIPROT Distinct T cell developmental consequences in humans and mice expressing identical mutations in the DLAARN motif of ZAP-70. 11123350

2001

dbSNP: rs104893674
rs104893674
0.700 GeneticVariation UNIPROT Specific immunoglobulin E responses in ZAP-70-deficient patients are mediated by Syk-dependent T-cell receptor signalling. 11412303

2001

dbSNP: rs137853201
rs137853201
0.700 GeneticVariation UNIPROT Distinct T cell developmental consequences in humans and mice expressing identical mutations in the DLAARN motif of ZAP-70. 11123350

2001

dbSNP: rs137853201
rs137853201
0.700 GeneticVariation UNIPROT Specific immunoglobulin E responses in ZAP-70-deficient patients are mediated by Syk-dependent T-cell receptor signalling. 11412303

2001

dbSNP: rs104893674
rs104893674
0.700 GeneticVariation UNIPROT ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency. 8202713

1994

dbSNP: rs104893674
rs104893674
0.700 GeneticVariation UNIPROT Defective T cell receptor signaling and CD8+ thymic selection in humans lacking zap-70 kinase. 8124727

1994

dbSNP: rs137853201
rs137853201
0.700 GeneticVariation UNIPROT ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency. 8202713

1994

dbSNP: rs137853201
rs137853201
0.700 GeneticVariation UNIPROT Defective T cell receptor signaling and CD8+ thymic selection in humans lacking zap-70 kinase. 8124727

1994

dbSNP: rs1254428002
rs1254428002
0.700 GeneticVariation UNIPROT