Variant: rs1555933851 

    present in Gene: ZC4H2
    present in Chromosome: X
    Position on Chromosome: 64919152
    Alleles of this Variant: -/G

rs1555933851 in ZC4H2 gene and Dysmorphic features PMID 23623388 2013 ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.

PMID 26056227 2015 ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons.

rs1555933851 in ZC4H2 gene and Multiple congenital anomalies PMID 26056227 2015 ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons.

PMID 23623388 2013 ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.