ClinVar Miner

Submissions for variant NC_000016.10:g.67660284T>C

dbSNP: rs2142976427
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002134725 SCV002413254 likely benign Dyskeratosis congenita, autosomal dominant 6 2021-09-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704758 SCV005218585 likely benign not provided criteria provided, single submitter not provided

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