FEZF1, FEZ family zinc finger 1, 389549

N. diseases: 73; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7779018
rs7779018
Entrez Id: 389549
Gene Symbol: FEZF1
FEZF1
CUI: C0036341
Disease:
Schizophrenia 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
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
dbSNP: rs587777739
rs587777739
Entrez Id: 154860;389549
Gene Symbol: FEZF1-AS1;FEZF1
FEZF1-AS1;FEZF1
CUI: C4017302
Disease:
HYPOGONADOTROPIC HYPOGONADISM 22 WITH ANOSMIA 		A 0.700 CausalMutation CLINVAR
dbSNP: rs587777740
rs587777740
Entrez Id: 154860;389549
Gene Symbol: FEZF1-AS1;FEZF1
FEZF1-AS1;FEZF1
CUI: C4017302
Disease:
HYPOGONADOTROPIC HYPOGONADISM 22 WITH ANOSMIA 		G 0.700 CausalMutation CLINVAR