Condition: Sparse and thin eyebrow


rs1555743003 in ASXL3 gene and Sparse and thin eyebrow PMID 27075689 2016 Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome.

rs779027563 in CNTNAP1 gene and Sparse and thin eyebrow PMID 27668699 2017 Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy.