ClinVar Miner

Submissions for variant NM_000122.2(ERCC3):c.111G>T (p.Ala37=)

dbSNP: rs749971925
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 RCV002159912 SCV002416567 likely benign not provided 2024-01-11 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002255727 SCV002532592 likely benign Xeroderma pigmentosum 2022-03-16 criteria provided, single submitter curation

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