Gene: LIN28B ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs221634
rs221634
LIN28B
0.010 GeneticVariation BEFREE We found genotype frequencies in rs314276 and rs221634 were significantly correlated with girls with CPP; while the C allele frequency in rs314276 showed the dominant trait. 28525351

2017
dbSNP: rs314276
rs314276
LIN28B
0.010 GeneticVariation BEFREE Our results demonstrate that the genotype of rs314276 in LIN28B is associated with girls with CPP, carrying dominant trait in the C allele. 28525351

2017
dbSNP: rs118000887
rs118000887
LIN28B
0.010 GeneticVariation BEFREE In vitro studies revealed that the rare LIN28B p.H199R variant identified in a girl with CPP does not affect the Lin28B function in the regulation of let-7 expression. 22964795

2012