ClinVar Miner

List of variants reported as benign for Charcot-Marie-Tooth disease type 4D

Included ClinVar conditions (1):
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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_006096.4(NDRG1):c.*956T>C rs1049697 0.83830
NM_006096.4(NDRG1):c.64-6T>C rs2272653 0.65276
NM_006096.4(NDRG1):c.538-132G>C rs2272650 0.41873
NM_006096.4(NDRG1):c.*691G>A rs1049694 0.32591
NM_006096.4(NDRG1):c.699-51A>C rs2233335 0.31793
NM_006096.4(NDRG1):c.450+61A>G rs2272651 0.29847
NM_006096.4(NDRG1):c.855+148T>C rs2233339 0.26454
NM_006096.4(NDRG1):c.756-5C>T rs2227262 0.11176
NM_006096.4(NDRG1):c.698+84A>G rs11575973 0.10802
NM_006096.4(NDRG1):c.891+39C>A rs2233341 0.09513
NM_006096.4(NDRG1):c.755+10T>C rs2233336 0.06123
NM_006096.4(NDRG1):c.*711C>T rs16904866 0.04897
NM_006096.4(NDRG1):c.*834T>A rs79281324 0.03589
NM_006096.4(NDRG1):c.*866A>T rs16904865 0.03230
NM_006096.4(NDRG1):c.*100G>A rs2233348 0.01904
NM_006096.4(NDRG1):c.*1135G>A rs10675 0.01865
NM_006096.4(NDRG1):c.892-5C>T rs2233346 0.01290
NM_006096.4(NDRG1):c.306C>T (p.Gly102=) rs2233322 0.01251
NM_006096.4(NDRG1):c.507G>A (p.Ala169=) rs2233331 0.01225
NM_006096.4(NDRG1):c.*69C>T rs114738844 0.01142
NM_006096.4(NDRG1):c.*1294T>C rs144034977 0.00858
NM_006096.4(NDRG1):c.199A>G (p.Met67Val) rs2233319 0.00829
NM_006096.4(NDRG1):c.879G>A (p.Pro293=) rs2233340 0.00458
NM_006096.4(NDRG1):c.-120C>T rs11575971
NM_006096.4(NDRG1):c.327-33C>T rs2233327
NM_006096.4(NDRG1):c.327-48C>G rs2233326

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