ClinVar Miner

List of variants in gene NDRG1 reported as likely benign by Molecular Genetics Laboratory, London Health Sciences Centre

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_006096.4(NDRG1):c.199A>G (p.Met67Val) rs2233319 0.00829
NM_006096.4(NDRG1):c.-18-2_-18-1del rs371927413 0.00490
NM_006096.4(NDRG1):c.879G>A (p.Pro293=) rs2233340 0.00458
NM_006096.4(NDRG1):c.331A>C (p.Met111Leu) rs2233328 0.00201
NM_006096.4(NDRG1):c.31G>A (p.Ala11Thr) rs145871479 0.00140
NM_006096.4(NDRG1):c.944-13C>T rs753312340 0.00039
NM_006096.4(NDRG1):c.1134G>A (p.Ser378=) rs750369546 0.00014
NM_006096.4(NDRG1):c.393G>A (p.Leu131=) rs149767690 0.00014
NM_006096.4(NDRG1):c.1053A>C (p.Arg351=) rs370153201 0.00010
NM_006096.4(NDRG1):c.594+9C>T rs373172944 0.00004
NM_006096.4(NDRG1):c.72C>T (p.Thr24=) rs551078982 0.00004
NM_006096.4(NDRG1):c.1062C>G (p.Ser354=) rs560162089 0.00003
NM_006096.4(NDRG1):c.100-3C>T rs775475505 0.00002
NM_006096.4(NDRG1):c.861G>A (p.Ala287=) rs150101908 0.00002
NM_006096.4(NDRG1):c.389+13G>C rs537705365 0.00001
NM_006096.4(NDRG1):c.1053_1082del (p.340TRSRSHTSEG[2]) rs751274009
NM_006096.4(NDRG1):c.206-17T>G rs1856694633
NM_006096.4(NDRG1):c.856-9C>T rs772996128
NM_006096.4(NDRG1):c.892-11G>A rs1855418193
NM_006096.4(NDRG1):c.973C>A (p.Arg325=) rs141078746

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