ClinVar Miner

Submissions for variant NM_032856.5(WDR73):c.1001A>G (p.Asp334Gly)

gnomAD frequency: 0.06616  dbSNP: rs72750868
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001663043 SCV001872343 benign not provided 2019-12-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001663043 SCV002407708 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243377 SCV002514951 benign Galloway-Mowat syndrome 1 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001663043 SCV005291978 benign not provided criteria provided, single submitter not provided

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