ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.662-10G>T

dbSNP: rs1554945255
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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 RCV000653810 SCV000775700 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2017-10-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507127 SCV002807035 likely benign Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; 11p partial monosomy syndrome 2022-05-03 criteria provided, single submitter clinical testing

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