ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.2811G>T (p.Lys937Asn)

gnomAD frequency: 0.00367  dbSNP: rs112454576
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000908162 SCV000530754 benign not provided 2018-09-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000908162 SCV001052909 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001821200 SCV002071109 uncertain significance not specified 2019-08-21 criteria provided, single submitter clinical testing

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