MLEC, malectin, 9761

N. diseases: 7; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2005455
rs2005455
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10431386
rs10431386
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs7306541
rs7306541
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs10431385
rs10431385
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs2005455
rs2005455
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs3829290
rs3829290
Entrez Id: 9761;105370029
Gene Symbol: MLEC;LOC105370029
MLEC;LOC105370029
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs7976497
rs7976497
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs10431386
rs10431386
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C0007789
Disease:
Cerebral Palsy 		0.010 GeneticVariation BEFREE The results of in vitro studies suggest that C alleles of rs10431386 and rs7964786 on MLEC promotes CP by inhibiting M1 to M2 macrophage polarization. 28972276 2018
dbSNP: rs7964786
rs7964786
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C0007789
Disease:
Cerebral Palsy 		0.010 GeneticVariation BEFREE The results of in vitro studies suggest that C alleles of rs10431386 and rs7964786 on MLEC promotes CP by inhibiting M1 to M2 macrophage polarization. 28972276 2018
dbSNP: rs7976497
rs7976497
Entrez Id: 9761
Gene Symbol: MLEC
MLEC
CUI: C2239176
Disease:
Liver carcinoma 		0.010 GeneticVariation BEFREE Polymorphisms of TLR4 rs2149356, AP3S2 rs2290351, STXBP5L rs2169302, MLEC rs7976497, and SOCS3 rs4969168 were associated with HCC risk in specific stratified analyses with gender, age, and drinking history in the cirrhotic patients. 27391584 2016