ClinVar Miner

Submissions for variant NC_000001.11:g.155301643del

gnomAD frequency: 0.04516  dbSNP: rs141119689
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001645114 SCV001859396 benign not provided 2021-06-20 criteria provided, single submitter clinical testing

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