CDA, cytidine deaminase, 978

N. diseases: 103; N. variants: 9
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs602950
rs602950 		0.925 0.080 1 20589038 upstream gene variant A/G snv 0.25
CUI: C0521585
Disease: Gastrointestinal mucositis
Gastrointestinal mucositis 		Digestive System Diseases; Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs602950
rs602950 		0.925 0.080 1 20589038 upstream gene variant A/G snv 0.25
CUI: C1167791
Disease: Skin toxicity
Skin toxicity 		0.010 1.000 1 2017 2017
dbSNP: rs139089160
rs139089160 		1 20592062 intron variant G/A;T snv
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2072671
rs2072671 		0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs2072671
rs2072671 		0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs2072671
rs2072671 		0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019