List of variants reported as uncertain significance for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1; Lateral meningocele syndrome; Myofibromatosis, infantile, 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000435.3(NOTCH3):c.*306C>T	rs181930934	0.00036
NM_000435.3(NOTCH3):c.2183G>A (p.Arg728His)	rs144935367	0.00024
NM_000435.3(NOTCH3):c.3227G>A (p.Arg1076His)	rs771803651	0.00008
NM_000435.3(NOTCH3):c.359C>T (p.Pro120Leu)	rs778715118	0.00006
NM_000435.3(NOTCH3):c.6619C>T (p.Arg2207Trp)	rs753170185	0.00006
NM_000435.3(NOTCH3):c.2960C>G (p.Thr987Ser)	rs752995216	0.00005
NM_000435.3(NOTCH3):c.451C>G (p.Gln151Glu)	rs371491165	0.00005
NM_000435.3(NOTCH3):c.6521G>A (p.Arg2174Gln)	rs1337328035	0.00005
NM_000435.3(NOTCH3):c.4914A>G (p.Glu1638=)	rs149222385	0.00003
NM_000435.3(NOTCH3):c.2051C>T (p.Pro684Leu)	rs770737365	0.00002
NM_000435.3(NOTCH3):c.119C>T (p.Ala40Val)	rs766139231	0.00001
NM_000435.3(NOTCH3):c.1783G>A (p.Gly595Ser)	rs770146452	0.00001
NM_000435.3(NOTCH3):c.21CCG[4] (p.Arg13del)	rs894374843
NM_000435.3(NOTCH3):c.4163C>T (p.Pro1388Leu)	rs1405393607
NM_000435.3(NOTCH3):c.6681C>G (p.His2227Gln)	rs1366113655

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