ClinVar Miner

Submissions for variant NM_020937.4(FANCM):c.4318-27G>A

gnomAD frequency: 0.19361  dbSNP: rs8020533
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001665882 SCV001881342 benign not provided 2019-02-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001703044 SCV001933303 benign Premature ovarian failure 15 2021-08-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702955 SCV001933304 benign Spermatogenic failure 28 2021-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001665882 SCV005289990 benign not provided criteria provided, single submitter not provided

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