List of variants in gene CNTNAP2 studied for Autism, susceptibility to, 15

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_014141.6(CNTNAP2):c.2099-26267A>G	rs2710102	0.56294
NM_014141.6(CNTNAP2):c.208+18133A>T	rs7794745	0.48010
NM_014141.6(CNTNAP2):c.2606T>C (p.Ile869Thr)	rs121908445	0.00016
NM_014141.6(CNTNAP2):c.1634C>T (p.Ala545Val)	rs771772546	0.00005
NM_014141.6(CNTNAP2):c.3047G>A (p.Arg1016Gln)	rs143879959	0.00001
NM_014141.6(CNTNAP2):c.3480_3481del (p.Gly1161fs)	rs771827120	0.00001
NM_014141.6(CNTNAP2):c.1238G>A (p.Ser413Asn)	rs796052371
NM_014141.6(CNTNAP2):c.3197A>G (p.Tyr1066Cys)	rs1795664797

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