SYT9, synaptotagmin 9, 143425

N. diseases: 11; N. variants: 3
Disease: Heart Septal Defects ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects 		0.010 GeneticVariation group BEFREE The intronic SYT9 variant rs11041321, which exhibits a significant genome-wide association with circulating homocysteine, was associated with the occurrence of CCSDs. 28834160 2017