Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199650082
rs199650082
0.010 GeneticVariation BEFREE We identified a missense SNP rs199650082 (2756G→A, R919Q, p = 1.4 × 10<sup>-6</sup>, odds ratio [OR] = 18.2, 95% confidence interval [CI] = 7.1-46.9) in an endoplasmic reticulum to the nucleus signaling-1 (ERN1) gene on chromosome 17 to be associated with DIH in the ARV-only cohort. 28388302

2017