rs1188383936, F2

N. diseases: 102
Disease: DiGeorge Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
DiGeorge Syndrome
CUI: C0012236
Disease: DiGeorge Syndrome
0.010 GeneticVariation BEFREE antiphospholipid antibodies syndrome associated with hyperhomocysteinemia related to MTHFR Gene C677T and A1298C heterozygous mutations in a young man with idiopathic hypoparathyroidism (DiGeorge syndrome). 16595601 2006