List of variants reported as uncertain significance for Huntington disease and related disorders by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_020655.4(JPH3):c.626G>C (p.Ser209Thr)	rs144296512	0.00143
NM_033305.3(VPS13A):c.7489C>T (p.Arg2497Cys)	rs762732340	0.00001
NM_001388492.1(HTT):c.8903G>A (p.Gly2968Asp)	rs1721646894
NM_020655.4(JPH3):c.2101dup (p.Gln701fs)

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