List of variants reported as uncertain significance for Nemaline myopathy 2 by Fulgent Genetics,Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP
NM_001271208.2(NEB):c.10181T>C (p.Ile3394Thr)	rs376182104
NM_001271208.2(NEB):c.10802A>G (p.His3601Arg)	rs371568550
NM_001271208.2(NEB):c.19966C>T (p.Arg6656Cys)	rs527250558
NM_001271208.2(NEB):c.20245C>A (p.Gln6749Lys)	rs772854423
NM_001271208.2(NEB):c.22099G>A (p.Val7367Ile)	rs189609282
NM_001271208.2(NEB):c.4904C>T (p.Thr1635Ile)	rs199662534

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