ClinVar Miner

Submissions for variant NM_001142800.2(EYS):c.160_162delinsAA (p.Tyr54fs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003468025 SCV004195221 likely pathogenic Retinitis pigmentosa 25 2023-08-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV003468025 SCV005672770 likely pathogenic Retinitis pigmentosa 25 2024-01-29 criteria provided, single submitter clinical testing

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