ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.308C>G (p.Ser103Ter)

dbSNP: rs147176389
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV001264295 SCV001442398 likely pathogenic Fanconi anemia complementation group A 2019-01-01 criteria provided, single submitter clinical testing
Baylor Genetics RCV001264295 SCV004196069 likely pathogenic Fanconi anemia complementation group A 2024-01-07 criteria provided, single submitter clinical testing

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