CHI3L1, chitinase 3 like 1, 1116

N. diseases: 420; N. variants: 9
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: rs6691378
rs6691378
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19
Secondary malignant neoplasm of lymph node
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs6691378
rs6691378
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs6691378
rs6691378
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs6691378
rs6691378
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19
CUI: C0677898
Disease: invasive cancer
invasive cancer
Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs6691378
rs6691378
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs6691378
rs6691378
0.882 0.160 1 203187994 upstream gene variant G/A snv 0.19
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs880633
rs880633
0.925 0.160 1 203183673 missense variant T/C snv 0.45 0.41
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs880633
rs880633
0.925 0.160 1 203183673 missense variant T/C snv 0.45 0.41
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017