ClinVar Miner

Submissions for variant NC_000001.11:g.100186848C>T

gnomAD frequency: 0.05990  dbSNP: rs4364901
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 RCV001671750 SCV001889904 benign not provided 2020-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001671750 SCV005283880 benign not provided criteria provided, single submitter not provided

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