ClinVar Miner

Submissions for variant NM_004629.1(FANCG):c.1636+7A>G (rs587118)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000247570 SCV000603581 benign not specified 2016-08-08 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000394450 SCV000479842 benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000367549 SCV000484367 benign Amyotrophic Lateral Sclerosis, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000275986 SCV000484368 benign Inclusion Body Myopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000247570 SCV000310552 benign not specified criteria provided, single submitter clinical testing

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