ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.13805T>C (p.Phe4602Ser)

dbSNP: rs574442439
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001243108 SCV001416244 likely benign not provided 2024-01-24 criteria provided, single submitter clinical testing
Natera, Inc. RCV001835154 SCV002088246 uncertain significance Usher syndrome type 2A 2019-11-06 no assertion criteria provided clinical testing

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