ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.655-29T>C

gnomAD frequency: 0.00240  dbSNP: rs182325576
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253211 SCV000306283 likely benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics RCV000992433 SCV001144743 benign not provided 2019-07-22 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000253211 SCV001156584 benign not specified 2019-05-23 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316368 SCV004016447 likely benign Neurofibromatosis, familial spinal 2023-07-07 criteria provided, single submitter clinical testing

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