rs1800692, TNFRSF1A

N. diseases: 5
Disease: ATRIAL SEPTAL DEFECT 1 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
ATRIAL SEPTAL DEFECT 1
CUI: C1862389
Disease: ATRIAL SEPTAL DEFECT 1
0.010 GeneticVariation BEFREE T-C polymorphism (rs1800692) was the only variation in the intron 4 of TNFRSF1A gene that we observed at the ASD patients. 23269568 2013