ClinVar Miner

Submissions for variant NM_024915.4(GRHL2):c.20+257del

dbSNP: rs1554579832
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Hardcastle Lab, UCL Institute of Ophthalmology RCV000656693 SCV000681415 likely pathogenic Corneal dystrophy 2018-02-02 no assertion criteria provided research

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