ClinVar Miner

Submissions for variant NM_003978.5(PSTPIP1):c.354+20C>A

dbSNP: rs184279306
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001423201 SCV001625774 likely benign Pyogenic arthritis-pyoderma gangrenosum-acne syndrome 2020-10-16 criteria provided, single submitter clinical testing
GeneDx RCV001597272 SCV001830289 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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