List of variants reported as uncertain significance for arthrogryposis multiplex congenita by Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001003722.2(GLE1):c.2029-5A>G	rs994582379	0.00004
NM_000113.3(TOR1A):c.20T>G (p.Val7Gly)	rs2031264115
NM_018684.4(ZC4H2):c.290_292del (p.Leu97del)

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