ClinVar Miner

Submissions for variant NM_005144.5(HR):c.1915+8A>G

dbSNP: rs1406164122
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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 RCV000949943 SCV001096219 likely benign not provided 2017-08-04 criteria provided, single submitter clinical testing

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