List of variants reported as uncertain significance for autosomal recessive degenerative and progressive cerebellar ataxia by Baylor Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_021830.5(TWNK):c.1042G>A (p.Gly348Arg)	rs62626271	0.00021
NM_021830.5(TWNK):c.2050A>C (p.Lys684Gln)	rs369223258	0.00009
NM_021830.5(TWNK):c.1975G>A (p.Ala659Thr)	rs370814108	0.00006
NM_000144.5(FXN):c.146C>A (p.Thr49Asn)	rs995690945	0.00004
NM_021830.5(TWNK):c.1958C>T (p.Ser653Phe)	rs775046032	0.00004
NM_021830.5(TWNK):c.1296G>T (p.Leu432Phe)	rs1382315425	0.00001
NM_022464.5(SIL1):c.741G>A (p.Ala247=)	rs773520401	0.00001
NM_004715.5(CTDP1):c.773-9T>G
NM_014053.4(FLVCR1):c.1516A>T (p.Ile506Leu)	rs1665131014
NM_014053.4(FLVCR1):c.236C>T (p.Ala79Val)	rs767746826
NM_021830.5(TWNK):c.2005G>A (p.Gly669Ser)	rs1851842282
NM_022464.5(SIL1):c.1012G>A (p.Asp338Asn)
NM_022464.5(SIL1):c.1238G>A (p.Arg413His)

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