ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.8845+1G>A

dbSNP: rs1553270954
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000669904 SCV000794704 likely pathogenic Usher syndrome type 2A; Retinitis pigmentosa 39 2017-10-24 criteria provided, single submitter clinical testing
Baylor Genetics RCV003472118 SCV004200686 likely pathogenic Retinitis pigmentosa 39 2023-06-08 criteria provided, single submitter clinical testing

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