ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.314+10T>G

dbSNP: rs1591718805
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 RCV000935432 SCV001081180 likely benign not provided 2018-04-08 criteria provided, single submitter clinical testing
Invitae RCV001496716 SCV001701426 likely benign Ataxia-telangiectasia-like disorder 2018-04-07 criteria provided, single submitter clinical testing

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