List of variants in gene CNTN1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001843.4(CNTN1):c.2598C>G (p.Ala866=)	rs140462332	0.00120
NM_001843.4(CNTN1):c.804-8A>G	rs56172264	0.00106
NM_001843.4(CNTN1):c.400+13T>C	rs201396853	0.00105
NM_001843.4(CNTN1):c.2823+5A>G	rs148453314	0.00078
NM_001843.4(CNTN1):c.873T>A (p.Ser291=)	rs200022020	0.00047
NM_001843.4(CNTN1):c.2824-6T>C	rs201098244	0.00010
NM_001843.4(CNTN1):c.2553A>G (p.Glu851=)	rs150210369	0.00004
NM_001843.4(CNTN1):c.882T>C (p.Val294=)	rs760650497	0.00002
NM_001843.4(CNTN1):c.1563C>T (p.Asn521=)	rs201595623
NM_001843.4(CNTN1):c.2184+9T>G
NM_001843.4(CNTN1):c.227+7T>C
NM_001843.4(CNTN1):c.2787T>G (p.Val929=)
NM_001843.4(CNTN1):c.401-14del	rs148387796
NM_001843.4(CNTN1):c.905T>C (p.Leu302Pro)	rs548330075

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