List of variants reported as uncertain significance for cerebellar ataxia by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_016373.4(WWOX):c.713A>G (p.Tyr238Cys)	rs142806268	0.00026
NM_014363.6(SACS):c.1941G>T (p.Lys647Asn)	rs201021919	0.00003
NM_001378615.1(CC2D2A):c.3601G>A (p.Gly1201Arg)	rs1392733763	0.00001
NM_016529.6(ATP8A2):c.1665G>A (p.Met555Ile)	rs1398724919	0.00001
NM_001447.3(FAT2):c.1521T>G (p.Ile507Met)	rs1758328376
NM_182961.4(SYNE1):c.13391A>G (p.Gln4464Arg)	rs2153973584

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