CX3CL1, C-X3-C motif chemokine ligand 1, 6376

N. diseases: 243; N. variants: 6
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: rs62037084
rs62037084 		16 57379748 missense variant C/T snv 5.1E-03 4.7E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs671623
rs671623 		16 57378890 5 prime UTR variant C/G snv 0.45
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8102
rs8102 		16 57384813 3 prime UTR variant C/T snv 0.70
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs170364
rs170364 		1.000 0.040 16 57376022 intron variant T/G snv 0.74
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.020 1.000 2 2015 2015
dbSNP: rs148601459
rs148601459 		0.925 0.200 16 57382838 missense variant G/A;T snv 1.4E-05; 4.6E-06
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs148601459
rs148601459 		0.925 0.200 16 57382838 missense variant G/A;T snv 1.4E-05; 4.6E-06
CUI: C0149517
Disease: Chronic tonsillitis
Chronic tonsillitis 		Infections; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs614230
rs614230 		1.000 0.040 16 57385374 downstream gene variant C/T snv 0.61
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs614230
rs614230 		1.000 0.040 16 57385374 downstream gene variant C/T snv 0.61
CUI: C0150055
Disease: Chronic pain
Chronic pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019