ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1776+10C>T

gnomAD frequency: 0.00001  dbSNP: rs767506133
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000873456 SCV001015451 likely benign Fanconi anemia 2024-10-16 criteria provided, single submitter clinical testing
Natera, Inc. RCV001271613 SCV001452880 likely benign Fanconi anemia complementation group A 2020-09-16 no assertion criteria provided clinical testing

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