ClinVar Miner

Submissions for variant NM_000083.3(CLCN1):c.799C>T (p.Leu267=)

dbSNP: rs1563075864
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000711238 SCV000841570 uncertain significance not provided 2017-12-12 criteria provided, single submitter clinical testing
Invitae RCV000711238 SCV001075910 likely benign not provided 2018-06-19 criteria provided, single submitter clinical testing

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