List of variants reported as likely benign for Huntington disease and related disorders by Fulgent Genetics, Fulgent Genetics

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001388492.1(HTT):c.7765+10G>A	rs79218467	0.03400
NM_001940.4(ATN1):c.1467G>A (p.Gln489=)	rs782253884	0.01283
NM_033305.3(VPS13A):c.9400-15A>C	rs117688596	0.00615
NM_033305.3(VPS13A):c.2037+8C>A	rs41289961	0.00417
NM_033305.3(VPS13A):c.1758T>C (p.Ala586=)	rs149037185	0.00199
NM_001388492.1(HTT):c.4638C>G (p.Val1546=)	rs116293982	0.00198
NM_020655.4(JPH3):c.1398T>C (p.Thr466=)	rs78661943	0.00194
NM_033305.3(VPS13A):c.4630+17A>G	rs371320559	0.00153
NM_033305.3(VPS13A):c.4041C>T (p.Ala1347=)	rs74983687	0.00113
NM_001386393.1(PANK2):c.291G>A (p.Lys97=)	rs764439399	0.00004
NM_033305.3(VPS13A):c.3075C>T (p.Ser1025=)	rs916979346	0.00002
NM_033305.3(VPS13A):c.8356A>C (p.Arg2786=)	rs752608628	0.00001
NM_001388492.1(HTT):c.99_100del (p.Gln34fs)
NM_001940.4(ATN1):c.1464GCA[14] (p.Gln502del)	rs60216939

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