ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.33C>T (p.Ser11=)

gnomAD frequency: 0.00010  dbSNP: rs376620550
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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 RCV000913926 SCV001059085 likely benign not provided 2024-10-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502754 SCV002808021 likely benign Galloway-Mowat syndrome 1 2021-11-20 criteria provided, single submitter clinical testing

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