ClinVar Miner

Submissions for variant NM_000223.4(KRT12):c.523G>A (p.Asp175Asn)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003455898 SCV004183325 benign Corneal dystrophy, Meesmann, 1 2023-12-12 criteria provided, single submitter research

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