List of variants reported as uncertain significance for Huntington disease and related disorders by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_033305.3(VPS13A):c.7850C>T (p.Pro2617Leu)	rs200293888	0.00004
NM_001128164.2(ATXN1):c.1804G>T (p.Ala602Ser)	rs1760808820
NM_001372574.1(ATXN2):c.1921A>C (p.Lys641Gln)	rs867381855
NM_033305.3(VPS13A):c.6485A>T (p.Asn2162Ile)	rs769503145

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