ClinVar Miner

Submissions for variant NM_004629.1(FANCG):c.881G>A (p.Gly294Glu) (rs17880082)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000228244 SCV000288631 likely benign Fanconi anemia 2019-12-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000502617 SCV000594710 uncertain significance not specified 2015-09-29 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000764833 SCV000895989 uncertain significance Fanconi anemia, complementation group G 2018-10-31 criteria provided, single submitter clinical testing

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