Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs375705600
rs375705600
Entrez Id: 7681
Gene Symbol: MKRN3
MKRN3
CUI: C0342544
Disease:
Idiopathic central precocious puberty
0.010 GeneticVariation BEFREE One paternally inherited rare variant, c.1034G>A (p.Arg345His), was identified in one girl with ICPP and in her brother with early puberty. 26331766 2015