ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.4110G>A (p.Gly1370=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003104511 SCV003780981 likely benign not provided 2022-08-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005029895 SCV005657913 uncertain significance Van Maldergem syndrome 2; Hennekam lymphangiectasia-lymphedema syndrome 2 2024-06-18 criteria provided, single submitter clinical testing

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