ClinVar Miner

Submissions for variant NM_004423.4(DVL3):c.2076G>A (p.Pro692=)

dbSNP: rs771367981
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003698723 SCV004473223 likely benign not provided 2023-06-20 criteria provided, single submitter clinical testing

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