ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.661+8G>A

gnomAD frequency: 0.00001  dbSNP: rs1313565005
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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 RCV001327234 SCV001518299 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2022-11-25 criteria provided, single submitter clinical testing
Mendelics RCV002246301 SCV002516756 benign not specified 2022-05-04 criteria provided, single submitter clinical testing

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