List of variants reported as likely pathogenic for arthrogryposis multiplex congenita by Mendelics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016213.5(TRIP4):c.925C>T (p.Arg309Ter)	rs147303485	0.00006
NM_018684.4(ZC4H2):c.199C>T (p.Arg67Ter)	rs1131691616
NM_173660.5(DOK7):c.957dup (p.Lys320fs)	rs794727884
NM_182895.5(SCARF2):c.915C>G (p.Cys305Trp)	rs1241075295

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