ClinVar Miner

Submissions for variant NM_004628.5(XPC):c.2033+57C>T

gnomAD frequency: 0.01096  dbSNP: rs3731141
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
GeneDx RCV001565874 SCV001789309 likely benign not provided 2019-11-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001565874 SCV005264620 likely benign not provided criteria provided, single submitter not provided

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