present in Gene: WNT7A
present in Chromosome: 3
Position on Chromosome: 13854777
Alleles of this Variant: C/T
rs104893832 in
WNT7A gene and
Fuhrmann syndrome
PMID 16826533 2006 Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.