IGLON5, IgLON family member 5, 402665

N. diseases: 16; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6509525
rs6509525
Entrez Id: 402665
Gene Symbol: IGLON5
IGLON5
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs35982135
rs35982135
Entrez Id: 402665
Gene Symbol: IGLON5
IGLON5
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018