List of variants reported as likely pathogenic for arthrogryposis multiplex congenita by Juno Genomics, Hangzhou Juno Genomics, Inc

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001378183.1(PIEZO2):c.8395C>G (p.Arg2799Gly)	rs587777451
NM_018668.5(VPS33B):c.290-1G>C
NM_182961.4(SYNE1):c.15438+2T>C
NM_182961.4(SYNE1):c.7642C>T (p.Gln2548Ter)

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