ClinVar Miner

Submissions for variant NM_001378452.1(ITPR1):c.279+18G>C

dbSNP: rs1266284169
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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 RCV002189896 SCV002342532 likely benign not provided 2021-04-24 criteria provided, single submitter clinical testing

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