List of variants reported as benign for Charcot-Marie-Tooth disease type 4B1 by Illumina Laboratory Services, Illumina

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_016156.6(MTMR2):c.1131C>T (p.Thr377=)	rs566204	0.28363
NM_016156.6(MTMR2):c.*1419G>A	rs496305	0.27825
NM_016156.6(MTMR2):c.*1934T>C	rs525404	0.27753
NM_016156.6(MTMR2):c.*1568C>T	rs596277	0.27751
NM_016156.6(MTMR2):c.*549G>A	rs611020	0.27729
NM_016156.6(MTMR2):c.8A>C (p.Lys3Thr)	rs3824874	0.27654
NM_016156.6(MTMR2):c.*1066T>C	rs16922622	0.07419
NM_016156.6(MTMR2):c.*1396C>T	rs16922615	0.07185
NM_016156.6(MTMR2):c.*1444C>G	rs149223349	0.04087
NM_016156.6(MTMR2):c.1756C>A (p.Arg586=)	rs61735577	0.04066
NM_016156.6(MTMR2):c.*2014T>G	rs112404010	0.03885
NM_016156.6(MTMR2):c.1504G>C (p.Glu502Gln)	rs61735578	0.03636
NM_016156.6(MTMR2):c.80+13C>T	rs139510268	0.01848
NM_016156.6(MTMR2):c.*2406C>T	rs16922613	0.01655
NM_016156.6(MTMR2):c.1233G>A (p.Thr411=)	rs113897932	0.01619
NM_016156.6(MTMR2):c.*1952G>A	rs118033833	0.01538
NM_016156.6(MTMR2):c.*85A>C	rs578159	0.01009
NM_016156.6(MTMR2):c.16A>T (p.Ser6Cys)	rs377006678	0.00014
NM_016156.6(MTMR2):c.*987T>C	rs57807625

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