ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.433+10A>G

gnomAD frequency: 0.00001  dbSNP: rs752878216
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001453956 SCV001657666 likely benign not provided 2023-05-31 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280036 SCV001467182 uncertain significance Usher syndrome type 3A 2020-08-14 no assertion criteria provided clinical testing

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