Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs774835569
rs774835569
Entrez Id: 3394;102466732
Gene Symbol: IRF8;MIR6774
IRF8;MIR6774
CUI: C4016741
Disease:
IMMUNODEFICIENCY 32B
T 0.700 CausalMutation CLINVAR