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.