CDA, cytidine deaminase, 978

N. diseases: 103; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3215400
rs3215400
Entrez Id: 978
Gene Symbol: CDA
CDA
CUI: C2745948
Disease:
Hyalinosis, Systemic
0.010 GeneticVariation BEFREE The deleted allele of rs3215400 shows an increased allele-specific expression and is significantly associated with an increased risk of capecitabine-induced HFS. 21325291 2011
dbSNP: rs532545
rs532545
Entrez Id: 978
Gene Symbol: CDA
CDA
CUI: C2745948
Disease:
Hyalinosis, Systemic
0.010 GeneticVariation BEFREE We found an association of HFS appearance with rs532545 located in the promoter region of CDD (OR = 2.02, 95% CI = 1.02-3.99, P = 0.039). 21325291 2011