ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3348+29C>T

gnomAD frequency: 0.00360  dbSNP: rs1800348
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254433 SCV000302490 likely benign not specified criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316334 SCV004017536 likely benign Fanconi anemia complementation group A 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705071 SCV005219756 likely benign not provided criteria provided, single submitter not provided

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