ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.5573-34del

dbSNP: rs35944387
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001645967 SCV001860044 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243353 SCV002514347 benign Retinitis pigmentosa 39 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243352 SCV002514359 benign Usher syndrome type 2A 2021-12-05 criteria provided, single submitter clinical testing

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