ClinVar Miner

Submissions for variant NC_000011.10:g.134068835C>G

gnomAD frequency: 0.03189  dbSNP: rs1940144
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 RCV001649845 SCV001867345 benign not provided 2018-07-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001649845 SCV005233983 benign not provided criteria provided, single submitter not provided

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