rs369831329, PROKR2

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypogonadism
CUI: C0020619
Disease: Hypogonadism
0.010 GeneticVariation BEFREE Recently, the homozygous mutation V274D was identified in a man displaying KS with an apparent reversal of hypogonadism. 23969157 2013
Kallmann Syndrome
CUI: C0162809
Disease: Kallmann Syndrome
0.010 GeneticVariation BEFREE Recently, the homozygous mutation V274D was identified in a man displaying KS with an apparent reversal of hypogonadism. 23969157 2013