Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204836
rs786204836
WNT5A
C 0.700 CausalMutation CLINVAR De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. 24716670

2015
dbSNP: rs786200925
rs786200925
WNT5A
G 0.700 CausalMutation CLINVAR WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918

2010
dbSNP: rs869312850
rs869312850
WNT5A
G 0.700 CausalMutation CLINVAR WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918

2010