ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.1084A>G (p.Thr362Ala)

dbSNP: rs2053319905
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001788958 SCV002030183 uncertain significance Fanconi anemia complementation group I 2021-11-26 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Fulgent Genetics, Fulgent Genetics RCV001788958 SCV002790856 uncertain significance Fanconi anemia complementation group I 2022-02-08 criteria provided, single submitter clinical testing

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