ClinVar Miner

Submissions for variant NM_004628.5(XPC):c.*156G>A

gnomAD frequency: 0.00006  dbSNP: rs121965092
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665491 SCV000789623 uncertain significance Xeroderma pigmentosum, group C 2017-02-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000665491 SCV000895536 uncertain significance Xeroderma pigmentosum, group C 2018-10-31 criteria provided, single submitter clinical testing

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