ZNF711, zinc finger protein 711, 7552

N. diseases: 52; N. variants: 9
Disease: Isolated somatotropin deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555970404
rs1555970404
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C3714796
Disease:
Isolated somatotropin deficiency 		TA 0.700 GeneticVariation CLINVAR Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705 2017
dbSNP: rs1555970404
rs1555970404
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C3714796
Disease:
Isolated somatotropin deficiency 		TA 0.700 GeneticVariation CLINVAR A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009