WNT7A, Wnt family member 7A, 7476

N. diseases: 182; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893832
rs104893832
Entrez Id: 7476
Gene Symbol: WNT7A
WNT7A
CUI: C0685381
Disease:
Congenital hypoplasia of radius
0.010 GeneticVariation BEFREE Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel (AA/RRS) phocomelia syndrome are rare autosomal recessive inherited disorders characterized by aplastic/hypoplastic nails with ectopic dorsal palms, absence of humeri, hypoplastic ulnae, and bowed short radii with the elbow joints present, shown to result from missense mutations in WNT7A (p.Ala109Thr and p.Arg292Cys). 21344627 2011
dbSNP: rs104893835
rs104893835
Entrez Id: 7476
Gene Symbol: WNT7A
WNT7A
CUI: C0685381
Disease:
Congenital hypoplasia of radius
0.010 GeneticVariation BEFREE Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel (AA/RRS) phocomelia syndrome are rare autosomal recessive inherited disorders characterized by aplastic/hypoplastic nails with ectopic dorsal palms, absence of humeri, hypoplastic ulnae, and bowed short radii with the elbow joints present, shown to result from missense mutations in WNT7A (p.Ala109Thr and p.Arg292Cys). 21344627 2011