ClinVar Miner

Submissions for variant NM_001098671.2(RASGRP2):c.1591+45T>G

gnomAD frequency: 0.72151  dbSNP: rs533515
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001652373 SCV001867935 benign not provided 2019-10-02 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796650 SCV002033452 benign Platelet-type bleeding disorder 18 2021-11-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001652373 SCV005319052 benign not provided criteria provided, single submitter not provided

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