ClinVar Miner

List of variants in gene NDRG1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006096.4(NDRG1):c.389+82G>T rs2233329 0.03173
NM_006096.4(NDRG1):c.699-295A>G rs141156426 0.01373
NM_006096.4(NDRG1):c.-18-204G>A rs76043183 0.01294
NM_006096.4(NDRG1):c.808-288G>A rs73364559 0.01293
NM_006096.4(NDRG1):c.*69C>T rs114738844 0.01142
NM_006096.4(NDRG1):c.891+61G>A rs2233342 0.01073
NM_006096.4(NDRG1):c.100-40A>T rs143266148 0.00965
NM_006096.4(NDRG1):c.390-309T>C rs76311337 0.00924
NM_006096.4(NDRG1):c.594+46C>T rs76569722 0.00895
NM_006096.4(NDRG1):c.891+283G>A rs148462369 0.00798
NM_006096.4(NDRG1):c.699-238T>C rs114771875 0.00778
NM_006096.4(NDRG1):c.450+155G>A rs1060400 0.00526
NM_006096.4(NDRG1):c.944-175A>C rs527246669 0.00498
NM_006096.4(NDRG1):c.855+180A>G rs190091490 0.00479
NM_006096.4(NDRG1):c.879G>A (p.Pro293=) rs2233340 0.00458
NM_006096.4(NDRG1):c.450+213A>G rs116510858 0.00421
NM_006096.4(NDRG1):c.*25G>A rs149804385 0.00419
NM_006096.4(NDRG1):c.206-106A>C rs2233321 0.00345
NM_006096.4(NDRG1):c.205+53G>A rs2233320 0.00344
NM_006096.4(NDRG1):c.63+227A>G rs191635379 0.00309
NM_006096.4(NDRG1):c.-19+92G>A rs571319753 0.00291
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.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.663C>T (p.Pro221=) rs377225752 0.00009
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.1155C>T (p.Ala385=) rs774605205 0.00004
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.808-6G>T rs779633074 0.00002
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.1077_1106dup (p.340TRSRSHTSEG[4]) rs1554747463
NM_006096.4(NDRG1):c.1095C>T (p.His365=) rs1278753145
NM_006096.4(NDRG1):c.327-114del rs113590255
NM_006096.4(NDRG1):c.64-20dup rs756038946
NM_006096.4(NDRG1):c.698+242C>T rs140613866
NM_006096.4(NDRG1):c.892-123C>A rs2233344
NM_006096.4(NDRG1):c.892-148_892-145del rs200823768
NM_006096.4(NDRG1):c.973C>A (p.Arg325=) rs141078746

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.