SLC2A1, solute carrier family 2 member 1, 6513

N. diseases: 687; N. variants: 76
Disease: Meningomyelocele ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		0.020 GeneticVariation disease BEFREE We detected an undertransmission for the SLC2A1 haplotype T-A (rs710218-rs2229682; P = .040), which was not significant when only lower MM (90% of the cases) was analyzed. 23427181 2013
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		0.020 GeneticVariation disease BEFREE A 10 bp deletion polymorphism and 2 new variations in the GLUT1 gene associated with meningomyelocele. 21135204 2011