List of variants reported as uncertain significance for Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis

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Total variants: 40

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.678G>C (p.Gln226His)	rs147282197	0.00056
NM_021830.5(TWNK):c.*709C>G	rs41291470	0.00046
NM_021830.5(TWNK):c.*453G>A	rs769950933	0.00040
NM_021830.5(TWNK):c.-592C>T	rs774214514	0.00026
NM_021830.5(TWNK):c.-418C>T	rs750659283	0.00015
NM_021830.5(TWNK):c.*341G>A	rs1007423847	0.00014
NM_021830.5(TWNK):c.-470G>A	rs886046626	0.00009
NM_021830.5(TWNK):c.-644A>T	rs886046623	0.00006
NM_021830.5(TWNK):c.*234T>G	rs886046633	0.00004
NM_021830.5(TWNK):c.*438G>C	rs886046634	0.00004
NM_021830.5(TWNK):c.*561C>T	rs901722933	0.00004
NM_021830.5(TWNK):c.*574C>T	rs886046636	0.00004
NM_021830.5(TWNK):c.-549G>A	rs886046625	0.00004
NM_021830.5(TWNK):c.1572C>T (p.His524=)	rs774091248	0.00004
NM_021830.5(TWNK):c.1597G>A (p.Ala533Thr)	rs139124415	0.00004
NM_021830.5(TWNK):c.*552G>C	rs111434414	0.00002
NM_021830.5(TWNK):c.*769G>A	rs919556945	0.00002
NM_021830.5(TWNK):c.922T>C (p.Leu308=)	rs754389465	0.00002
NM_021830.5(TWNK):c.*367A>G	rs62626296	0.00001
NM_021830.5(TWNK):c.*619G>A	rs886046637	0.00001
NM_021830.5(TWNK):c.*763T>C	rs886046639	0.00001
NM_021830.5(TWNK):c.1196A>G (p.Asn399Ser)	rs863223921	0.00001
NM_021830.5(TWNK):c.1853C>T (p.Pro618Leu)	rs886046632	0.00001
NM_021830.5(TWNK):c.913G>A (p.Val305Ile)	rs753457416	0.00001
NM_002693.3(POLG):c.1811C>T (p.Ala604Val)	rs1433922299
NM_021830.5(TWNK):c.*248G>A	rs1851850715
NM_021830.5(TWNK):c.*346A>C	rs1851852761
NM_021830.5(TWNK):c.*555G>A	rs886046635
NM_021830.5(TWNK):c.*747C>G	rs886046638
NM_021830.5(TWNK):c.-304G>A	rs200599543
NM_021830.5(TWNK):c.-423C>T	rs886046627
NM_021830.5(TWNK):c.-584G>C	rs1564806518
NM_021830.5(TWNK):c.-585T>G	rs886046624
NM_021830.5(TWNK):c.-622C>T	rs993449080
NM_021830.5(TWNK):c.1070G>C (p.Arg357Pro)	rs758026634
NM_021830.5(TWNK):c.1826G>T (p.Arg609Leu)	rs1274226715
NM_021830.5(TWNK):c.1906G>A (p.Ala636Thr)	rs1426435572
NM_021830.5(TWNK):c.276C>T (p.Gly92=)	rs886046631
NM_021830.5(TWNK):c.596G>A (p.Arg199Gln)	rs1564807938
NM_021830.5(TWNK):c.77G>T (p.Gly26Val)	rs772221026

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