Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556004813
rs1556004813
A 0.700 CausalMutation CLINVAR Next-generation sequencing in X-linked intellectual disability. 25649377

2015

dbSNP: rs1556004813
rs1556004813
A 0.700 CausalMutation CLINVAR Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. 26350204

2015

dbSNP: rs1556004813
rs1556004813
A 0.700 CausalMutation CLINVAR Expanding the clinical phenotype of patients with a ZDHHC9 mutation. 24357419

2014

dbSNP: rs1556004813
rs1556004813
A 0.700 CausalMutation CLINVAR A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009

dbSNP: rs1556004813
rs1556004813
A 0.700 CausalMutation CLINVAR Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus. 17436253

2007