ClinVar Miner

Submissions for variant NM_025132.4(WDR19):c.603+23C>T

gnomAD frequency: 0.96807  dbSNP: rs1451817
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001656635 SCV001865383 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243370 SCV002514750 benign Cranioectodermal dysplasia 4 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243369 SCV002514751 benign Nephronophthisis 13 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243371 SCV002514752 benign Senior-Loken syndrome 8 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243368 SCV002514754 benign Asphyxiating thoracic dystrophy 5 2021-12-05 criteria provided, single submitter clinical testing

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