CCL4, C-C motif chemokine ligand 4, 6351

N. diseases: 276; 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: rs10491121
rs10491121 		0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs10491121
rs10491121 		0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs10491121
rs10491121 		0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs10491121
rs10491121 		0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs10491121
rs10491121 		0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1049807
rs1049807 		1.000 0.080 17 36105270 missense variant A/G snv 0.22 0.21
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs1719152
rs1719152 		1.000 0.080 17 36105271 missense variant T/A snv 0.21 0.18
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia 		Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1719153
rs1719153 		1.000 0.120 17 36105836 upstream gene variant A/T snv 0.17
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2018 2018