C9, complement C9, 735

N. diseases: 62; N. variants: 32
Disease: C9 Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34000044
rs34000044
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C3151189
Disease:
C9 Deficiency 		T 0.700 GeneticVariation CLINVAR Utilization of genomic sequencing for population screening of immunodeficiencies in the newborn. 28617419 2017
dbSNP: rs34000044
rs34000044
Entrez Id: 735
Gene Symbol: C9
C9
CUI: C3151189
Disease:
C9 Deficiency 		T 0.700 CausalMutation CLINVAR