ZNF711, zinc finger protein 711, 7552

N. diseases: 52; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060505033
rs1060505033
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.800 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705 2017
dbSNP: rs1060505033
rs1060505033
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.800 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009
dbSNP: rs1060505033
rs1060505033
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		C 0.800 CausalMutation CLINVAR
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: C0026351
Disease:
Moderate intellectual disability 		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: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		TA 0.700 GeneticVariation CLINVAR Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705 2017
dbSNP: rs367654949
rs367654949
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.700 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705 2017
dbSNP: rs760346140
rs760346140
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.700 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705 2017
dbSNP: rs777239465
rs777239465
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.700 GeneticVariation UNIPROT 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
dbSNP: rs1555970404
rs1555970404
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		TA 0.700 GeneticVariation CLINVAR A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009
dbSNP: rs1555970404
rs1555970404
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C0026351
Disease:
Moderate intellectual disability 		TA 0.700 GeneticVariation CLINVAR A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009
dbSNP: rs367654949
rs367654949
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.700 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009
dbSNP: rs760346140
rs760346140
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.700 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009
dbSNP: rs777239465
rs777239465
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		0.700 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009
dbSNP: rs1060505032
rs1060505032
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1060505033
rs1060505033
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C1843367
Disease:
Poor school performance 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1555974716
rs1555974716
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C1843367
Disease:
Poor school performance 		GA 0.700 GeneticVariation CLINVAR
dbSNP: rs1555974716
rs1555974716
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		GA 0.700 GeneticVariation CLINVAR
dbSNP: rs199422240
rs199422240
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C2749020
Disease:
Mental Retardation, X-Linked, Znf711-Related 		T 0.700 CausalMutation CLINVAR
dbSNP: rs768314738
rs768314738
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C0235831
Disease:
Renal Cell Dysplasia 		0.010 GeneticVariation BEFREE A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome. 19723756 2009
dbSNP: rs768314738
rs768314738
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C3536714
Disease:
Renal dysplasia 		0.010 GeneticVariation BEFREE A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome. 19723756 2009