List of variants in gene CIC reported as likely benign for Autism spectrum disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001386298.1(CIC):c.1975C>T (p.Arg659Cys)	rs2036866760
NM_001386298.1(CIC):c.2131_2150delinsACGAT (p.Pro711_Glu717delinsThrMet)	rs2513610208
NM_001386298.1(CIC):c.7018A>C (p.Lys2340Gln)	rs2514083473

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