Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122868
rs398122868
Entrez Id: 732
Gene Symbol: C8B
C8B
CUI: C3151080
Disease:
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
GCACAGCC 0.700 CausalMutation CLINVAR