Variant: rs1569339085 

    present in Gene: ASXL1
    present in Chromosome: 20
    Position on Chromosome: 32436772
    Alleles of this Variant: G/T

rs1569339085 in ASXL1 gene and Bohring syndrome PMID 26633542 2016 Clinical application of whole-exome sequencing across clinical indications.

PMID 25131622 2014 Clinical whole exome sequencing in child neurology practice.