ClinVar Miner

Submissions for variant NM_004628.5(XPC):c.90GGA[6] (p.Glu34dup)

dbSNP: rs750450365
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666792 SCV000791148 uncertain significance Xeroderma pigmentosum, group C 2017-05-04 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV001508139 SCV001714091 uncertain significance not provided 2019-10-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000666792 SCV002815127 uncertain significance Xeroderma pigmentosum, group C 2022-05-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001508139 SCV005187535 uncertain significance not provided criteria provided, single submitter not provided

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