Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773694113
rs773694113
AT 0.700 CausalMutation CLINVAR Clinical efficacy of a next-generation sequencing gene panel for primary immunodeficiency diagnostics. 29077208

2018

dbSNP: rs1560679469
rs1560679469
GA 0.700 GeneticVariation CLINVAR

dbSNP: rs1560711146
rs1560711146
A 0.700 GeneticVariation CLINVAR

dbSNP: rs869320688
rs869320688
G 0.700 CausalMutation CLINVAR

dbSNP: rs869320689
rs869320689
G 0.700 CausalMutation CLINVAR

dbSNP: rs869320754
rs869320754
GA 0.700 CausalMutation CLINVAR