Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1449441916
rs1449441916
C3
0.700 GeneticVariation UNIPROT Inherited human complement C3 deficiency. An amino acid substitution in the beta-chain (ASP549 to ASN) impairs C3 secretion. 7961791

1994
dbSNP: rs1568229677
rs1568229677
C3
A 0.700 CausalMutation CLINVAR