ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.497-14C>T

gnomAD frequency: 0.00001  dbSNP: rs2497190635
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003817215 SCV004618710 likely benign not provided 2024-10-25 criteria provided, single submitter clinical testing

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