ClinVar

Description

Variant summary: WNT1 c.506dupG (p.Cys170LeufsX6) results in a premature termination codon, predicted to cause a truncation of the encoded protein or absence of the protein due to nonsense mediated decay, which are commonly known mechanisms for disease. Truncations downstream of this position have been classified as pathogenic in ClinVar. The variant allele was found at a frequency of 9.5e-05 in 232192 control chromosomes. This frequency is not significantly higher than expected for a pathogenic variant in WNT1 causing Osteogenesis Imperfecta (9.5e-05 vs 0.0011), allowing no conclusion about variant significance. c.506dupG has been reported in the literature in multiple individuals affected with Osteogenesis Imperfecta. These data indicate that the variant is very likely to be associated with disease. One clinical diagnostic laboratory has submitted clinical-significance assessments for this variant to ClinVar after 2014 without evidence for independent evaluation and classified the variant as pathogenic. Based on the evidence outlined above, the variant was classified as pathogenic.