ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.845+7G>A

gnomAD frequency: 0.00001  dbSNP: rs767339664
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
Invitae RCV000458066 SCV000558623 likely benign not provided 2016-07-08 criteria provided, single submitter clinical testing
Invitae RCV001462097 SCV001666008 likely benign Ataxia-telangiectasia-like disorder 2016-07-05 criteria provided, single submitter clinical testing

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