ClinVar Miner

Submissions for variant NM_001378452.1(ITPR1):c.3565-17T>C

dbSNP: rs760881384
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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 RCV002092407 SCV002326238 likely benign not provided 2021-11-17 criteria provided, single submitter clinical testing

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