List of variants reported as uncertain significance for X-linked disease by Institute of Human Genetics, University of Goettingen

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_031407.7(HUWE1):c.2570C>T (p.Pro857Leu)	rs782526786	0.00004
NM_000390.4(CHM):c.1714G>A (p.Val572Ile)	rs2148120495
NM_000489.6(ATRX):c.6504+5_6504+14del	rs2064891953
NM_000539.3(RHO):c.194_205del (p.His65_Leu68del)
NM_001008537.3(NEXMIF):c.907C>G (p.Leu303Val)	rs2080115822
NM_001032382.2(PQBP1):c.313C>T (p.Arg105Trp)	rs1222724041
NM_001079872.2(CUL4B):c.2650G>A (p.Asp884Asn)	rs1922994124
NM_001110556.2(FLNA):c.4525G>A (p.Val1509Ile)	rs782018054
NM_001830.4(CLCN4):c.1439G>T (p.Gly480Val)	rs2147182640
NM_003491.4(NAA10):c.30C>G (p.Asp10Glu)	rs2148536720
NM_004187.5(KDM5C):c.1583+5G>T	rs2073531540
NM_005334.3(HCFC1):c.5782G>A (p.Ala1928Thr)
NM_005391.5(PDK3):c.836A>G (p.Glu279Gly)	rs2148201759
NM_006013.5(RPL10):c.218A>C (p.Asn73Thr)	rs2148138707
NM_080632.3(UPF3B):c.711AGA[2] (p.Glu240del)	rs2056156815

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