Variant: rs864309676 

    present in Gene: STX7
    present in Chromosome: 6
    Position on Chromosome: 132472372
    Alleles of this Variant: T/G

rs864309676 in STX7 gene and Infantile Spasm PMID 26395554 2016 Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.

rs864309676 in STX7 gene and Malformations of Cortical Development, Group II PMID 26395554 2016 Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.

rs864309676 in STX7 gene and Microcephaly (physical finding) PMID 26395554 2016 Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.

rs864309676 in STX7 gene and Neuronal heterotopia PMID 26395554 2016 Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.

rs864309676 in STX7 gene and Pachygyria PMID 26395554 2016 Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.

rs864309676 in STX7 gene and Poor school performance PMID 26395554 2016 Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.

rs864309676 in STX7 gene and Seizures PMID 26395554 2016 Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.