List of variants reported as benign for Charcot-Marie-Tooth disease axonal type 2N by Illumina Laboratory Services, Illumina

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Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_001605.3(AARS1):c.2715T>C (p.Val905=)	rs4081753	0.85676
NM_001605.3(AARS1):c.903C>T (p.His301=)	rs2070203	0.49332
NM_001605.3(AARS1):c.671+3A>G	rs74024185	0.07668
NM_001605.3(AARS1):c.824G>A (p.Gly275Asp)	rs11537667	0.07667
NM_001605.3(AARS1):c.*74A>T	rs11537663	0.05921
NM_001605.3(AARS1):c.*251A>C	rs116553521	0.01298
NM_001605.3(AARS1):c.2900A>T (p.Lys967Met)	rs35744709	0.00971
NM_001605.3(AARS1):c.2791G>A (p.Gly931Ser)	rs149377346	0.00718
NM_001605.3(AARS1):c.1404C>T (p.Tyr468=)	rs117598688	0.00646
NM_001605.3(AARS1):c.1685C>T (p.Thr562Ile)	rs148355156	0.00591
NM_001605.3(AARS1):c.64G>A (p.Glu22Lys)	rs151091410	0.00568
NM_001605.3(AARS1):c.1672-4T>A	rs187509039	0.00236
NM_001605.3(AARS1):c.2521-3C>T	rs200586605	0.00190
NM_001605.3(AARS1):c.*141A>G	rs576707006	0.00161
NM_001605.3(AARS1):c.700C>T (p.Pro234Ser)	rs141840552	0.00137
NM_001605.3(AARS1):c.1332G>A (p.Glu444=)	rs150442667	0.00096
NM_001605.3(AARS1):c.2608-6C>A	rs200965527	0.00088
NM_001605.3(AARS1):c.2185C>T (p.Arg729Trp)	rs138081804	0.00072
NM_001605.3(AARS1):c.1044G>C (p.Thr348=)	rs181264712	0.00067
NM_001605.3(AARS1):c.1428G>C (p.Arg476=)	rs80257731	0.00041
NM_001605.3(AARS1):c.741G>A (p.Leu247=)	rs148075561	0.00038
NM_001605.3(AARS1):c.561C>T (p.Cys187=)	rs78523270	0.00019
NM_001605.3(AARS1):c.1481G>T (p.Ser494Ile)	rs771059047	0.00003
NM_001605.3(AARS1):c.904G>A (p.Ala302Thr)	rs576221121	0.00001

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