ClinVar Miner

Submissions for variant NM_170665.4(ATP2A2):c.2030G>C (p.Arg677Pro)

dbSNP: rs1879294675
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV001839191 SCV002099134 uncertain significance Acrokeratosis verruciformis of Hopf; Keratosis follicularis 2021-03-21 criteria provided, single submitter clinical testing

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