CXCL1, C-X-C motif chemokine ligand 1, 2919

N. diseases: 315; N. variants: 3
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: rs3117603
rs3117603 		4 73867841 upstream gene variant A/T snv 0.45
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4074
rs4074 		0.827 0.200 4 73870427 intron variant A/G snv 0.46
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		Pathological Conditions, Signs and Symptoms 0.020 1.000 2 2012 2013
dbSNP: rs4074
rs4074 		0.827 0.200 4 73870427 intron variant A/G snv 0.46
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.020 1.000 2 2012 2013
dbSNP: rs3117604
rs3117604 		1.000 0.080 4 73868951 upstream gene variant T/C snv 0.47
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4074
rs4074 		0.827 0.200 4 73870427 intron variant A/G snv 0.46
CUI: C0023891
Disease: Liver Cirrhosis, Alcoholic
Liver Cirrhosis, Alcoholic 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Chemically-Induced Disorders 0.010 1.000 1 2013 2013
dbSNP: rs4074
rs4074 		0.827 0.200 4 73870427 intron variant A/G snv 0.46
CUI: C0023895
Disease: Liver diseases
Liver diseases 		Digestive System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4074
rs4074 		0.827 0.200 4 73870427 intron variant A/G snv 0.46
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs4074
rs4074 		0.827 0.200 4 73870427 intron variant A/G snv 0.46
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2012 2012