ClinVar Miner

Submissions for variant NM_174878.3(CLRN1):c.291C>T (p.Ile97=)

gnomAD frequency: 0.00001  dbSNP: rs1231233910
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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
Counsyl RCV000672035 SCV000797090 uncertain significance Usher syndrome type 3 2018-01-11 criteria provided, single submitter clinical testing
Invitae RCV001495848 SCV001700538 likely benign not provided 2023-05-18 criteria provided, single submitter clinical testing

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