List of variants in gene CNTNAP2 reported as uncertain significance by New York Genome Center

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_014141.6(CNTNAP2):c.2609T>C (p.Val870Ala)	rs138481453	0.00096
NM_014141.6(CNTNAP2):c.2369G>A (p.Arg790His)	rs73464271	0.00086
NM_014141.6(CNTNAP2):c.479G>A (p.Arg160His)	rs138738227	0.00048
NM_014141.6(CNTNAP2):c.1879G>A (p.Val627Ile)	rs147447659	0.00029
NM_014141.6(CNTNAP2):c.3154C>T (p.Arg1052Cys)	rs139930720	0.00016
NM_014141.6(CNTNAP2):c.102A>C (p.Lys34Asn)	rs779436784	0.00003
NM_014141.6(CNTNAP2):c.3577G>A (p.Ala1193Thr)	rs751491210	0.00001
NM_014141.6(CNTNAP2):c.2384-4637del	rs2116601181
NM_014141.6(CNTNAP2):c.3076G>A (p.Ala1026Thr)	rs796052382

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