ClinVar Miner

List of variants in gene NDRG1 studied for not specified

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_006096.4(NDRG1):c.64-6T>C rs2272653 0.65276
NM_006096.4(NDRG1):c.-19+367G>T rs77890421 0.07116
NM_006096.4(NDRG1):c.892-5C>T rs2233346 0.01290
NM_006096.4(NDRG1):c.507G>A (p.Ala169=) rs2233331 0.01225
NM_006096.4(NDRG1):c.199A>G (p.Met67Val) rs2233319 0.00829
NM_006096.4(NDRG1):c.122A>G (p.His41Arg) rs2233318 0.00054
NM_006096.4(NDRG1):c.944-13C>T rs753312340 0.00039
NM_006096.4(NDRG1):c.-19+14C>G rs886062716 0.00029
NM_006096.4(NDRG1):c.393G>A (p.Leu131=) rs149767690 0.00014
NM_006096.4(NDRG1):c.*2C>T rs200367524 0.00013
NM_006096.4(NDRG1):c.-8G>A rs200465804 0.00010
NM_006096.4(NDRG1):c.874C>A (p.Leu292Ile) rs745520295 0.00010
NM_006096.4(NDRG1):c.663C>T (p.Pro221=) rs377225752 0.00009
NM_006096.4(NDRG1):c.1051C>T (p.Arg351Ter) rs765621411 0.00008
NM_006096.4(NDRG1):c.1101C>T (p.Ser367=) rs201959970 0.00007
NM_006096.4(NDRG1):c.*18C>T rs1008102394 0.00006
NM_006096.4(NDRG1):c.129T>C (p.Ser43=) rs758024351 0.00003
NM_006096.4(NDRG1):c.1152C>T (p.Ser384=) rs863224413 0.00002
NM_006096.4(NDRG1):c.1070G>C (p.Ser357Thr) rs1290016868 0.00001
NM_006096.4(NDRG1):c.595-12C>T rs751730957 0.00001
NM_006096.4(NDRG1):c.891+15G>A rs1554748576 0.00001
NM_006096.4(NDRG1):c.965G>A (p.Arg322His) rs1307068606 0.00001
NM_006096.4(NDRG1):c.1095C>T (p.His365=) rs1278753145
NM_006096.4(NDRG1):c.595-6A>G rs1554749794
NM_006096.4(NDRG1):c.964C>T (p.Arg322Cys) rs368404338
NM_006096.4(NDRG1):c.973C>A (p.Arg325=) rs141078746

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