Variant: rs886037864 

    present in Gene: BCL11A
    present in Chromosome: 2
    Position on Chromosome: 60546217
    Alleles of this Variant: T/G

rs886037864 in BCL11A gene and INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN PMID 27453576 2016 BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.

PMID 30250039 2018 Functional characterization of TBR1 variants in neurodevelopmental disorder.