ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1150_1163del (p.Val384fs)

dbSNP: rs2143529990
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Kariminejad - Najmabadi Pathology & Genetics Center RCV001814564 SCV001755632 pathogenic Abnormality of blood and blood-forming tissues 2021-07-10 criteria provided, single submitter clinical testing

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