ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.4143A>T (p.Glu1381Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003148557 SCV003835634 uncertain significance Hennekam lymphangiectasia-lymphedema syndrome 2 2022-05-12 criteria provided, single submitter clinical testing
Baylor Genetics RCV003148556 SCV003835679 uncertain significance Van Maldergem syndrome 2 2022-05-12 criteria provided, single submitter clinical testing

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