ATF3, activating transcription factor 3, 467

N. diseases: 228; N. variants: 4
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: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs3123543
rs3123543 		1 212617344 intron variant T/A;C snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs10475
rs10475 		1.000 0.080 1 212620271 3 prime UTR variant T/C snv 0.76
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs11119982
rs11119982 		1.000 0.080 1 212591502 intron variant C/T snv 0.40
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension 		Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1365908231
rs1365908231 		0.925 0.120 1 212619442 missense variant A/C snv
CUI: C0848558
Disease: Hypospadias
Hypospadias 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1365908231
rs1365908231 		0.925 0.120 1 212619442 missense variant A/C snv
CUI: C1691215
Disease: Penile hypospadias
Penile hypospadias 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2008 2008