Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs192636495
rs192636495
0.010 GeneticVariation BEFREE Although two of them were novel, those polymorphisms could not lead to amino acid changes. p.P110T was detected less frequently in CPP patients than in the controls (P = 0.022). 20631455

2010

dbSNP: rs201073751
rs201073751
0.010 GeneticVariation BEFREE The p.H90D mutation was identified in the homozygous state in two unrelated girls with CPP. 20237166

2010

dbSNP: rs587777843
rs587777843
0.010 GeneticVariation BEFREE The p.P74S mutation was identified in the heterozygous state in a boy who developed CPP at 1 yr of age. 20237166

2010