List of variants reported as uncertain significance for cerebral arterial disease by Fulgent Genetics, Fulgent Genetics

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001613.4(ACTA2):c.977C>A (p.Thr326Asn)	rs777832794	0.00003
NM_001613.4(ACTA2):c.129+5G>A	rs373402293	0.00002
NM_001613.4(ACTA2):c.203C>T (p.Thr68Ile)	rs1060500132	0.00001
NM_001613.4(ACTA2):c.296C>G (p.Ala99Gly)	rs779757924	0.00001
NM_001613.4(ACTA2):c.553C>T (p.Arg185Ter)	rs772473154	0.00001
NM_001613.4(ACTA2):c.689C>G (p.Ala230Gly)	rs757461793	0.00001
NM_001256071.3(RNF213):c.15251C>T (p.Ala5084Val)
NM_001256071.3(RNF213):c.8714C>T (p.Pro2905Leu)
NM_001613.4(ACTA2):c.129+4A>G	rs1390177518
NM_001613.4(ACTA2):c.78C>A (p.Asp26Glu)	rs141538225

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