ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3765+37G>A

gnomAD frequency: 0.05858  dbSNP: rs34420680
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000242361 SCV000302496 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001640468 SCV001858036 benign not provided 2019-02-02 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316338 SCV004017543 benign Fanconi anemia complementation group A 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001640468 SCV005253294 benign not provided criteria provided, single submitter not provided

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