List of variants in gene CNTNAP2 reported as uncertain significance by Athena Diagnostics Inc

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_014141.6(CNTNAP2):c.73G>A (p.Ala25Thr)	rs200866893	0.00101
NM_014141.6(CNTNAP2):c.479G>A (p.Arg160His)	rs138738227	0.00048
NM_014141.6(CNTNAP2):c.400T>G (p.Trp134Gly)	rs139694086	0.00021
NM_014141.6(CNTNAP2):c.2606T>C (p.Ile869Thr)	rs121908445	0.00018
NM_014141.6(CNTNAP2):c.755-5C>T	rs369675346	0.00010
NM_014141.6(CNTNAP2):c.3112G>A (p.Asp1038Asn)	rs144003410	0.00006
NM_014141.6(CNTNAP2):c.3179C>T (p.Ala1060Val)	rs369254596	0.00006
NM_014141.6(CNTNAP2):c.3833C>T (p.Thr1278Ile)	rs760047247	0.00003
NM_014141.6(CNTNAP2):c.2440A>G (p.Thr814Ala)	rs1060503571
NM_014141.6(CNTNAP2):c.3193C>A (p.Leu1065Ile)	rs146225600
NM_014141.6(CNTNAP2):c.3555C>G (p.Asn1185Lys)	rs369699763
NM_014141.6(CNTNAP2):c.638C>T (p.Ala213Val)	rs1563079216

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