ClinVar Miner

List of variants in gene CNTNAP2 reported as pathogenic for autism, susceptiblity to

Included ClinVar conditions (22):

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_014141.6(CNTNAP2):c.2497del (p.Trp833fs)	rs1391540245	0.00001
NM_014141.6(CNTNAP2):c.3480_3481del (p.Gly1161fs)	rs771827120	0.00001

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