rs1946519 is a SNP of the IL18 gene. It is significantly associated with altered IL18, TNFA, IL6, IL18/IL10 and TNFA/IL10 (cytokines) ratio levels [R].
rs1946519 (no reported alleles) is associated with recurrent spontaneous miscarriage (RSM) [R].
The ''C'' allele was associated with an increased risk of acute myocardial infarction (AMI) [R].
Women with AC+AA genotype are at relatively high risk for cervical cancer [R].
The ''C'' allele was more frequent in type 1 diabetes (T1D) patients [R].