Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060505033
rs1060505033
ZNF711
0.800 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705

2017
dbSNP: rs1060505033
rs1060505033
ZNF711
0.800 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009
dbSNP: rs1060505033
rs1060505033
ZNF711
C 0.800 CausalMutation CLINVAR

dbSNP: rs1555970404
rs1555970404
ZNF711
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
ZNF711
0.700 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705

2017
dbSNP: rs760346140
rs760346140
ZNF711
0.700 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705

2017
dbSNP: rs777239465
rs777239465
ZNF711
0.700 GeneticVariation UNIPROT Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705

2017
dbSNP: rs1555970404
rs1555970404
ZNF711
TA 0.700 GeneticVariation CLINVAR A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009
dbSNP: rs367654949
rs367654949
ZNF711
0.700 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009
dbSNP: rs760346140
rs760346140
ZNF711
0.700 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009
dbSNP: rs777239465
rs777239465
ZNF711
0.700 GeneticVariation UNIPROT A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009
dbSNP: rs1060505032
rs1060505032
ZNF711
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555974716
rs1555974716
ZNF711
GA 0.700 GeneticVariation CLINVAR

dbSNP: rs199422240
rs199422240
ZNF711
T 0.700 CausalMutation CLINVAR