List of variants reported as likely pathogenic for cerebellar disorder by New York Genome Center

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001163809.2(WDR81):c.2567C>T (p.Pro856Leu)	rs587776906	0.00007
NM_025114.4(CEP290):c.6645+1G>A	rs201218801	0.00005
NM_001134831.2(AHI1):c.430del (p.Glu144fs)	rs2128098409
NM_001378452.1(ITPR1):c.4691T>C (p.Leu1564Pro)	rs2125272771
NM_015215.4(CAMTA1):c.4690-2A>G	rs2523695759
NM_018294.6(CWF19L1):c.942del (p.Pro315fs)	rs749679347

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