Gene: SOHLH1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 402381
Gene Symbol: SOHLH1
SOHLH1 		0.110 GeneticVariation disease CLINVAR Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism. 25774885 2015
Entrez Id: 402381
Gene Symbol: SOHLH1
SOHLH1 		0.110 GeneticVariation disease BEFREE Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism. 25774885 2015