List of variants in gene CIC reported as likely pathogenic for central nervous system neoplasm

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001386298.1(CIC):c.3017_3018insT (p.Gly1008fs)	rs1568503055
NM_001386298.1(CIC):c.3370C>T (p.Arg1124Trp)	rs1568504941

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