ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.2613+8dup

dbSNP: rs2150739145
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
Invitae RCV001485522 SCV001689958 likely benign CHARGE association 2020-10-06 criteria provided, single submitter clinical testing

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