List of variants reported as uncertain significance for Huntington disease and related disorders by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001388492.1(HTT):c.2108C>T (p.Pro703Leu)	rs768047421	0.00004
NM_001388492.1(HTT):c.6250G>A (p.Gly2084Arg)	rs780493120	0.00003
NM_001388492.1(HTT):c.7498G>A (p.Val2500Ile)	rs371399733	0.00003
NM_001128164.2(ATXN1):c.641_642insTCAGCA (p.Gln213_Gln214insHisGln)
NM_001372574.1(ATXN2):c.682T>G (p.Leu228Val)
NM_033305.3(VPS13A):c.3943C>A (p.Gln1315Lys)

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