ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.336C>G (p.Thr112=)

dbSNP: rs565400473
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000668143 SCV000792694 likely benign Usher syndrome type 3 2017-07-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000979978 SCV001127926 likely benign not provided 2024-03-25 criteria provided, single submitter clinical testing

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