ClinVar Miner

Submissions for variant NM_025132.4(WDR19):c.717-11C>G

dbSNP: rs1370589827
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811704 SCV002049355 likely benign not provided 2021-06-11 criteria provided, single submitter clinical testing
Invitae RCV003772208 SCV004569275 likely benign Asphyxiating thoracic dystrophy 5; Senior-Loken syndrome 8 2024-01-19 criteria provided, single submitter clinical testing

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