ClinVar Miner

Submissions for variant NM_014915.3(ANKRD26):c.-118C>A

dbSNP: rs1589393759
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV001003519 SCV001161825 likely pathogenic Thrombocytopenia no assertion criteria provided research

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