List of variants reported as likely pathogenic for arthrogryposis multiplex congenita by Centogene AG - the Rare Disease Company

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001198800.3(ASCC1):c.583C>T (p.Gln195Ter)	rs769501930	0.00001
NM_018684.4(ZC4H2):c.174_178del (p.Glu58fs)	rs2147349682
NM_139284.3(LGI4):c.1272C>A (p.Cys424Ter)	rs2065136111
NM_139284.3(LGI4):c.263_265del (p.Phe88del)	rs2065190797

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