List of variants reported as likely benign for cerebellar dysfunction with variable cognitive and behavioral abnormalities by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015215.4(CAMTA1):c.2730A>G (p.Ser910=)	rs6674962	0.00613
NM_015215.4(CAMTA1):c.986A>G (p.Lys329Arg)	rs151133441	0.00433
NM_015215.4(CAMTA1):c.3066+20C>T	rs147462930	0.00264
NM_015215.4(CAMTA1):c.1955C>T (p.Ser652Leu)	rs144242373	0.00137

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