List of variants reported as uncertain significance for Charcot-Marie-Tooth disease, demyelinating, IIA 1I

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_018082.6(POLR3B):c.3390G>C (p.Lys1130Asn)	rs201527706	0.00009
NM_018082.6(POLR3B):c.1324C>T (p.Arg442Cys)	rs1442212683	0.00001
NM_018082.6(POLR3B):c.2740G>A (p.Glu914Lys)	rs1381339891	0.00001
NM_018082.6(POLR3B):c.2899A>C (p.Ser967Arg)	rs200865021	0.00001
NM_018082.6(POLR3B):c.1346T>C (p.Leu449Pro)	rs2137002042
NM_018082.6(POLR3B):c.1757C>T (p.Ser586Phe)	rs2542118888
NM_018082.6(POLR3B):c.1996G>A (p.Gly666Ser)
NM_018082.6(POLR3B):c.2024C>T (p.Pro675Leu)
NM_018082.6(POLR3B):c.2045G>A (p.Arg682Lys)	rs2137017154
NM_018082.6(POLR3B):c.2644A>C (p.Lys882Gln)
NM_018082.6(POLR3B):c.627G>T (p.Glu209Asp)
NM_018082.6(POLR3B):c.634A>G (p.Ser212Gly)

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