ClinVar Miner

Submissions for variant NM_013296.5(GPSM2):c.954-19G>T

dbSNP: rs17030744
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001586604 SCV001814034 likely benign not provided 2019-01-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001586604 SCV002376967 benign not provided 2023-12-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001586604 SCV005259230 likely benign not provided criteria provided, single submitter not provided

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