ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1777-41_1777-38del

dbSNP: rs56163653
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
PreventionGenetics, part of Exact Sciences RCV000244065 SCV000302465 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV002247691 SCV002520172 likely benign not provided 2019-06-21 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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