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

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_001005373.4(LRSAM1):c.1974T>C (p.Ser658=)	rs140336379	0.00065
NM_001005373.4(LRSAM1):c.406+15G>T	rs201808404	0.00064
NM_001005373.4(LRSAM1):c.586G>A (p.Gly196Ser)	rs148059394	0.00045
NM_001005373.4(LRSAM1):c.1225C>G (p.Gln409Glu)	rs149540339	0.00039
NM_001005373.4(LRSAM1):c.917T>G (p.Leu306Arg)	rs140151379	0.00039
NM_001005373.4(LRSAM1):c.2111G>A (p.Arg704His)	rs140808447	0.00035
NM_001005373.4(LRSAM1):c.1950G>A (p.Thr650=)	rs199887448	0.00029
NM_001005373.4(LRSAM1):c.569G>A (p.Arg190Gln)	rs142782210	0.00020
NM_001005373.4(LRSAM1):c.*590T>C	rs139260397	0.00017
NM_001005373.4(LRSAM1):c.94G>A (p.Asp32Asn)	rs150784835	0.00017
NM_001005373.4(LRSAM1):c.1601C>T (p.Thr534Met)	rs141542114	0.00015
NM_001005373.4(LRSAM1):c.751-8C>G	rs367823841	0.00011
NM_001005373.4(LRSAM1):c.1153G>A (p.Val385Ile)	rs373570877	0.00009
NM_001005373.4(LRSAM1):c.1746G>A (p.Ser582=)	rs199997686	0.00009
NM_001005373.4(LRSAM1):c.480C>T (p.Asn160=)	rs147205387	0.00009
NM_001005373.4(LRSAM1):c.458G>A (p.Arg153His)	rs368689811	0.00005
NM_001005373.4(LRSAM1):c.1141C>T (p.Arg381Trp)	rs763390117	0.00004
NM_001005373.4(LRSAM1):c.1382A>T (p.Gln461Leu)	rs145382004	0.00004
NM_001005373.4(LRSAM1):c.685G>A (p.Glu229Lys)	rs563259179	0.00004
NM_001005373.4(LRSAM1):c.954C>T (p.Asn318=)	rs200527839	0.00004
NM_001005373.4(LRSAM1):c.1504-5C>G	rs377190920	0.00003
NM_001005373.4(LRSAM1):c.284C>T (p.Ala95Val)	rs570248730	0.00001
NM_001005373.4(LRSAM1):c.1351G>A (p.Ala451Thr)	rs202166023
NM_001005373.4(LRSAM1):c.1930G>T (p.Gly644Cys)	rs201284198
NM_001005373.4(LRSAM1):c.706G>A (p.Asp236Asn)	rs551957380

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