FEZF1, FEZ family zinc finger 1, 389549

N. diseases: 73; N. variants: 3
Disease: HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777739
rs587777739
Entrez Id: 154860;389549
Gene Symbol: FEZF1-AS1;FEZF1
FEZF1-AS1;FEZF1
CUI: C4014988
Disease:
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA 		0.700 GeneticVariation UNIPROT Mutations in FEZF1 cause Kallmann syndrome. 25192046 2014