ClinVar Miner

Submissions for variant NM_004628.5(XPC):c.537-8_537-5del

dbSNP: rs1210551886
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001415078 SCV001617227 likely benign not provided 2024-01-19 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258235 SCV002537520 uncertain significance Xeroderma pigmentosum 2021-12-01 criteria provided, single submitter curation

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