Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122522
rs398122522
0.800 GeneticVariation UNIPROT Mutant prolactin receptor and familial hyperprolactinemia. 24195502

2013

dbSNP: rs398122522
rs398122522
C 0.800 CausalMutation CLINVAR

dbSNP: rs376188691
rs376188691
A 0.700 CausalMutation CLINVAR

dbSNP: rs754974807
rs754974807
A 0.700 CausalMutation CLINVAR

dbSNP: rs1799836
rs1799836
0.010 GeneticVariation BEFREE One statistically significant association between polymorphic variant rs1799836 of MAOB gene and HPRL in men was found in the total group. 30967134

2019

dbSNP: rs3863145
rs3863145
0.010 GeneticVariation BEFREE Furthermore, the rs40184 and rs3863145 variants in SLC6A3 gene appeared to be associated with HPRL in the subgroup of patients using the risperidone/paliperidone, but not with HPRL induced by other antipsychotic drugs. 30967134

2019

dbSNP: rs40184
rs40184
0.010 GeneticVariation BEFREE Furthermore, the rs40184 and rs3863145 variants in SLC6A3 gene appeared to be associated with HPRL in the subgroup of patients using the risperidone/paliperidone, but not with HPRL induced by other antipsychotic drugs. 30967134

2019

dbSNP: rs1341239
rs1341239
0.010 GeneticVariation BEFREE This study revealed a significant association between the polymorphic variant rs1341239 and the development of hyperprolactinemia in patients with schizophrenia. 27776952

2017

dbSNP: rs17326429
rs17326429
0.010 GeneticVariation BEFREE This study revealed an association between HPRL and X-chromosome haplotypes comprised of the rs569959 and rs17326429 polymorphisms. 27654063

2017

dbSNP: rs569959
rs569959
0.010 GeneticVariation BEFREE This study revealed an association between HPRL and X-chromosome haplotypes comprised of the rs569959 and rs17326429 polymorphisms. 27654063

2017

dbSNP: rs6318
rs6318
0.010 GeneticVariation BEFREE Considering both sexes together and also specifically among females, the occurrence of hyperprolactinemia was higher in the presence of the C allele of the rs6318 single nucleotide polymorphisms (SNP) of the HTR2C gene. 26682995

2015