ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.666A>G (p.Gln222=)

dbSNP: rs1567794382
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001470648 SCV001674745 likely benign Fanconi anemia complementation group O 2021-12-24 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV000936071 SCV001365269 uncertain significance not provided 2016-11-12 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Andreas Laner.

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