List of variants in gene CNTN1 reported as 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.1416C>T (p.Asn472=)	rs1056019	0.62528
NM_001843.4(CNTN1):c.1014T>C (p.Asn338=)	rs935105	0.13920
NM_001843.4(CNTN1):c.2711-17A>G	rs12367345	0.12247
NM_001843.4(CNTN1):c.1805-14C>A	rs10784981	0.11616
NM_001843.4(CNTN1):c.1893T>C (p.His631=)	rs2229929	0.03763
NM_001843.4(CNTN1):c.1956A>G (p.Ala652=)	rs2229930	0.03222
NM_001843.4(CNTN1):c.401-9C>T	rs57340925	0.02401
NM_001843.4(CNTN1):c.2324G>A (p.Ser775Asn)	rs34326474	0.00980
NM_001843.4(CNTN1):c.2670A>T (p.Gly890=)	rs34346038	0.00972
NM_001843.4(CNTN1):c.90T>C (p.His30=)	rs61748365	0.00707
NM_001843.4(CNTN1):c.2493T>C (p.His831=)	rs61754102	0.00396
NM_001843.4(CNTN1):c.1401T>C (p.Gly467=)	rs61759480	0.00215
NM_001843.4(CNTN1):c.2980+19A>T	rs181426756	0.00112
NM_001843.4(CNTN1):c.2785G>A (p.Val929Ile)	rs148239965	0.00006

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