List of variants reported as uncertain significance for arthrogryposis syndrome by Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000079.4(CHRNA1):c.191A>C (p.Asp64Ala)
NM_001164508.2(NEB):c.22639A>G (p.Met7547Val)
NM_020654.5(SENP7):c.3088C>T (p.Arg1030Trp)

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