Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776823
rs587776823
Entrez Id: 757;3460
Gene Symbol: TMEM50B;IFNGR2
TMEM50B;IFNGR2
CUI: C4013947
Disease:
IMMUNODEFICIENCY 28
A 0.700 CausalMutation CLINVAR