ClinVar Miner

Submissions for variant NM_002303.6(LEPR):c.1604-16T>C

gnomAD frequency: 0.00202  dbSNP: rs143936245
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001663439 SCV001879817 likely benign not specified 2020-12-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002539640 SCV003031901 benign not provided 2023-07-03 criteria provided, single submitter clinical testing

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