rs1165860389, NUP107

N. diseases: 2
Disease: Primary hypogonadism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Primary hypogonadism
CUI: C0948896
Disease: Primary hypogonadism
0.010 GeneticVariation BEFREE Our findings indicate that NUP107 R355C variant falls in the category of variant of unknown significance as the cause of HH and infertility. 29363275 2018