List of variants reported as uncertain significance for arthrogryposis multiplex congenita 2, neurogenic type by Baylor Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_018668.5(VPS33B):c.1780A>G (p.Arg594Gly)	rs868354713	0.00004
NM_001193315.2(VIPAS39):c.494G>A (p.Arg165Gln)	rs376797384	0.00001
NM_018668.5(VPS33B):c.44T>C (p.Phe15Ser)	rs748609085	0.00001
NM_001193315.2(VIPAS39):c.1003A>G (p.Thr335Ala)	rs867268041
NM_001193315.2(VIPAS39):c.1366G>A (p.Asp456Asn)	rs2078466084
NM_018668.5(VPS33B):c.572C>G (p.Pro191Arg)	rs770015890

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