CCL22, C-C motif chemokine ligand 22, 6367

N. diseases: 182; N. variants: 5
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: rs223889
rs223889 		1.000 0.080 16 57358329 upstream gene variant T/C snv 0.59
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs41398344
rs41398344 		16 57360481 missense variant T/C snv 5.2E-03 4.7E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs223818
rs223818 		0.925 0.080 16 57360846 intron variant C/G snv 0.77
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs223818
rs223818 		0.925 0.080 16 57360846 intron variant C/G snv 0.77
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs223888
rs223888 		1.000 0.080 16 57357856 upstream gene variant A/G;T snv
CUI: C0003615
Disease: Appendicitis
Appendicitis 		Digestive System Diseases; Infections 0.010 1.000 1 2020 2020
dbSNP: rs4359426
rs4359426 		0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4359426
rs4359426 		0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2017 2017
dbSNP: rs4359426
rs4359426 		0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.010 1.000 1 2017 2017