ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.785-7T>G

dbSNP: rs758280375
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001954464 SCV002196582 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-11-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004010886 SCV004832552 uncertain significance Wilms tumor 1 2023-06-26 criteria provided, single submitter clinical testing This variant causes a T to G nucleotide substitution at the -7 position in intron 2 of the WT1 gene. To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with hereditary cancer in the literature. This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

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