CCL2, C-C motif chemokine ligand 2, 6347

N. diseases: 1157; N. variants: 8
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: rs3760396
rs3760396 		0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15
CUI: C0279557
Disease: Adenosquamous cell lung cancer
Adenosquamous cell lung cancer 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3760396
rs3760396 		0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		Neoplasms 0.010 < 0.001 1 2016 2016
dbSNP: rs3760396
rs3760396 		0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3760396
rs3760396 		0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3760396
rs3760396 		0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3917887
rs3917887 		0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal 		Infections; Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4586
rs4586 		0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2857656
rs2857656 		0.851 0.120 17 34254988 upstream gene variant G/A;C snv
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2017 2017
dbSNP: rs2857656
rs2857656 		0.851 0.120 17 34254988 upstream gene variant G/A;C snv
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2017 2017
dbSNP: rs2857656
rs2857656 		0.851 0.120 17 34254988 upstream gene variant G/A;C snv
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2017 2017
dbSNP: rs4586
rs4586 		0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs13900
rs13900 		0.925 0.120 17 34256892 3 prime UTR variant C/T snv 0.28
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs4586
rs4586 		0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2019 2019
dbSNP: rs13900
rs13900 		0.925 0.120 17 34256892 3 prime UTR variant C/T snv 0.28
CUI: C0023283
Disease: Leishmaniasis, Cutaneous
Leishmaniasis, Cutaneous 		Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2020 2020