ClinVar Miner

Submissions for variant NM_001098671.2(RASGRP2):c.371+5G>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV003447760 SCV004175473 uncertain significance Platelet-type bleeding disorder 18 2022-07-15 criteria provided, single submitter clinical testing

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