Condition: Broad eyebrow


rs1060499548 in ABL1 gene and Broad eyebrow PMID 28288113 2017 Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations.

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