Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2069705
rs2069705
IFNG ; IFNG-AS1
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		0.010 GeneticVariation BEFREE Haplotype analyses identified a three-marker risk IFNG haplotype rs2069727-rs2069718-rs2069705 associated with SIDS (OR = 1.62, 95% CI 1.23-2.13; p = 0.0003). 30617847

2019