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.