LGALS2, galectin 2, 3957

N. diseases: 27; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2281097
rs2281097
Entrez Id: 3957
Gene Symbol: LGALS2
LGALS2
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs1434020843
rs1434020843
Entrez Id: 3957
Gene Symbol: LGALS2
LGALS2
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.700 GeneticVariation UNIPROT
dbSNP: rs7291467
rs7291467
Entrez Id: 3957
Gene Symbol: LGALS2
LGALS2
CUI: C0027051
Disease:
Myocardial Infarction
0.020 GeneticVariation BEFREE A putative risk genotype of the polymorphism in the LGALS2 gene (rs7291467; 3279T/C) was not associated with myocardial infarction (OR 0.98, 95% CI 0.83-1.16; P = 0.84). 17517687 2007
dbSNP: rs7291467
rs7291467
Entrez Id: 3957
Gene Symbol: LGALS2
LGALS2
CUI: C0027051
Disease:
Myocardial Infarction
0.020 GeneticVariation BEFREE LGALS2 functional variant rs7291467 is not associated with susceptibility to myocardial infarction in Caucasians. 17098239 2007
dbSNP: rs7291467
rs7291467
Entrez Id: 3957
Gene Symbol: LGALS2
LGALS2
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE PPARG rs1152002, AGTR1 rs5186, CXCL16 rs3744700 and LGALS2 rs7291467 polymorphisms may be closely related to the development of CHD. 26045830 2015
dbSNP: rs7291467
rs7291467
Entrez Id: 3957
Gene Symbol: LGALS2
LGALS2
CUI: C2747816
Disease:
Complicated malaria
0.010 GeneticVariation BEFREE We tested the association between rs7291467, a single-nucleotide polymorphism (SNP) in the LTalpha-related gene encoding galectin-2 (LGALS2), disease severity, and function in a case-control study of ethnic Highland Papuan adults and children with SM (n = 380) and asymptomatic malaria-exposed controls (n = 356) originating from a non-malaria-endemic region but residing in a lowland malaria-endemic area of Papua, Indonesia. 20500087 2010
dbSNP: rs7291467
rs7291467
Entrez Id: 3957
Gene Symbol: LGALS2
LGALS2
CUI: C0007785
Disease:
Cerebral Infarction
0.010 GeneticVariation BEFREE The Chi-square test, multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the prevalence of hypertension, hypercholesterolemia, and diabetes mellitus, as well as a stepwise forward selection procedure revealed that the 2445G-->A (Ala54Thr) polymorphism (rs1799883) of FABP2, the -108/3G-->4G polymorphism of IPF1 (S82168), the A-->G (Thr94Ala) polymorphism (rs2241883) of FABP1, the G-->A (Asp2213Asn) polymorphism (rs529038) of ROS1, the -11377C-->G polymorphism (rs266729) of ADIPOQ, the 162A-->C polymorphism (rs4769055) of ALOX5AP, the -786T-->C polymorphism (rs2070744) of NOS3, and the 3279C-->T polymorphism (rs7291467) of LGALS2 were associated (P<0.05) with the prevalence of atherothrombotic cerebral infarction. 18506375 2008