ClinVar Miner

Submissions for variant NM_000082.4(ERCC8):c.482-17C>T

gnomAD frequency: 0.00034  dbSNP: rs201126529
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
PreventionGenetics, part of Exact Sciences RCV000253138 SCV000301995 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057296 SCV002347000 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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