Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2814778
rs2814778
0.030 GeneticVariation BEFREE Individuals homozygous for the C allele at rs2814778 were significantly more likely to develop neutropenia and have to stop clozapine treatment (OR = 20.4, P = 3.44 × 10<sup>-7</sup>). 30647433

2019

dbSNP: rs2814778
rs2814778
0.030 GeneticVariation BEFREE Healthy individuals of African ancestry have neutropenia that has been linked with the variant rs2814778(G) of the gene encoding atypical chemokine receptor 1 (ACKR1). 28553950

2017

dbSNP: rs2814778
rs2814778
0.030 GeneticVariation BEFREE Further research is needed on the associations of rs2814778 genotype with neutropenia and treatment delay in the setting of cancer. 18710383

2008