ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3822C>A (p.Thr1274=)

dbSNP: rs1382340096
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001487035 SCV001691518 likely benign Fanconi anemia 2020-09-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501673 SCV002811981 likely benign Fanconi anemia complementation group A 2021-09-29 criteria provided, single submitter clinical testing

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