LGALS2, galectin 2, 3957

N. diseases: 27; N. variants: 3
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: rs2281097
rs2281097 		22 37570053 downstream gene variant T/C snv 0.50
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1434020843
rs1434020843 		1.000 0.080 22 37570268 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs7291467
rs7291467 		0.851 0.160 22 37576621 intron variant G/A snv 0.49
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 < 0.001 2 2007 2007
dbSNP: rs7291467
rs7291467 		0.851 0.160 22 37576621 intron variant G/A snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs7291467
rs7291467 		0.851 0.160 22 37576621 intron variant G/A snv 0.49
CUI: C2747816
Disease: Complicated malaria
Complicated malaria 		Infections 0.010 1.000 1 2010 2010
dbSNP: rs7291467
rs7291467 		0.851 0.160 22 37576621 intron variant G/A snv 0.49
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2008 2008