rs7180942, NTRK3

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Eating Disorders
CUI: C0013473
Disease: Eating Disorders
0.010 GeneticVariation BEFREE Interestingly, HapMap unrelated individuals carrying the rs7180942 risk genotypes for ED showed higher levels of expression of NTRK3 in lymphoblastoid cell lines. 18203754 2008