ClinVar Miner

Submissions for variant NM_002109.6(HARS1):c.730-10G>C

dbSNP: rs1581505929
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001506723 SCV001711657 likely benign Usher syndrome type 3B 2018-07-03 criteria provided, single submitter clinical testing

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