ClinVar Miner

Submissions for variant NM_001082486.2(ACD):c.413+7G>A

dbSNP: rs1017802690
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001494806 SCV001699471 likely benign Dyskeratosis congenita, autosomal dominant 6 2020-08-28 criteria provided, single submitter clinical testing

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