ClinVar Miner

Submissions for variant NM_017934.7(PHIP):c.601-4T>C

dbSNP: rs202141638
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002214825 SCV002364051 benign not provided 2022-11-17 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002214825 SCV005051180 likely benign not provided 2024-05-01 criteria provided, single submitter clinical testing PHIP: BP4, BS1

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