ClinVar Miner

Submissions for variant NM_003025.4(SH3GL1):c.771C>G (p.Pro257=)

dbSNP: rs243261
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001637606 SCV001850894 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807455 SCV002055189 benign Acute myeloid leukemia 2021-07-15 criteria provided, single submitter clinical testing

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