List of variants reported as uncertain significance for cerebellar dysfunction with variable cognitive and behavioral abnormalities by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015215.4(CAMTA1):c.2227G>A (p.Gly743Arg)	rs965685976	0.00001
NM_015215.4(CAMTA1):c.2473A>G (p.Ser825Gly)	rs765488241
NM_015215.4(CAMTA1):c.511-22_511-19del	rs2095751767
NM_015215.4(CAMTA1):c.851G>A (p.Arg284His)	rs767725186

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