ClinVar Miner

Submissions for variant NM_003978.5(PSTPIP1):c.-421CCTG[8]

dbSNP: rs55909412
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000314841 SCV000393981 benign Pyogenic arthritis-pyoderma gangrenosum-acne syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001683277 SCV001903213 benign not provided 2019-08-21 criteria provided, single submitter clinical testing

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