rs1137100, LEPR

N. diseases: 39
Disease: Meningomyelocele ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
0.010 GeneticVariation BEFREE In addition, the leptin receptor rs1137100 G allele showed a significant increase in the risk of MM for maternal-derived alleles in the whole sample (2.43-fold; P = .038) and in lower MM (3.20-fold; P = .014). 23427181 2013