Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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|
0.800 | GeneticVariation | UNIPROT | Mutant prolactin receptor and familial hyperprolactinemia. | 24195502 | 2013 |
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C | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
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 |
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|
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 |
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|
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 |
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|
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 |
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|
0.010 | GeneticVariation | BEFREE | This study revealed an association between HPRL and X-chromosome haplotypes comprised of the rs569959 and rs17326429 polymorphisms. | 27654063 | 2017 |
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|
0.010 | GeneticVariation | BEFREE | This study revealed an association between HPRL and X-chromosome haplotypes comprised of the rs569959 and rs17326429 polymorphisms. | 27654063 | 2017 |
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|
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 |