ClinVar Miner

Submissions for variant NM_153816.6(SNX14):c.516T>C (p.Phe172=)

gnomAD frequency: 0.00133  dbSNP: rs143497401
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000883208 SCV001026496 benign not provided 2023-10-06 criteria provided, single submitter clinical testing
GeneDx RCV000883208 SCV001771442 likely benign not provided 2018-09-17 criteria provided, single submitter clinical testing

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