ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3408+33T>C

gnomAD frequency: 0.01875  dbSNP: rs17227191
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246376 SCV000302491 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711648 SCV001941195 benign not provided 2019-04-24 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316335 SCV004017556 benign Fanconi anemia complementation group A 2023-07-07 criteria provided, single submitter clinical testing

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