ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.710-10G>A

dbSNP: rs2040524006
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV001256222 SCV002786743 uncertain significance Fanconi anemia complementation group A 2022-03-17 criteria provided, single submitter clinical testing
Baylor Genetics RCV001256222 SCV004196635 likely pathogenic Fanconi anemia complementation group A 2022-05-15 criteria provided, single submitter clinical testing
Leiden Open Variation Database RCV001256222 SCV001425627 uncertain significance Fanconi anemia complementation group A 2020-02-28 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Sue Richards.

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