ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3163C>A (p.Arg1055=)

dbSNP: rs753063086
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001964354 SCV002250778 likely benign Fanconi anemia 2024-10-25 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003323965 SCV004030026 likely benign not specified 2023-07-24 criteria provided, single submitter clinical testing

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