Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1861493
rs1861493
IFNG ; IFNG-AS1
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		0.010 GeneticVariation BEFREE AA allele frequencies of rs1861493 were also associated with a significantly higher risk of CAA in KD patients. 27124053

2016