ClinVar Miner

List of variants reported as uncertain significance for Nemaline myopathy 7 by Revvity Omics, Revvity

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_138638.5(CFL2):c.73A>G (p.Thr25Ala)	rs1004680147	0.00001
NM_138638.5(CFL2):c.230T>G (p.Leu77Arg)
NM_138638.5(CFL2):c.327A>G (p.Ala109=)
NM_138638.5(CFL2):c.500A>G (p.Ter167=)

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