List of variants reported as benign for EEM syndrome by Genome-Nilou Lab

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001793.6(CDH3):c.390+37T>C	rs2296410	0.87073
NM_001793.6(CDH3):c.720G>A (p.Thr240=)	rs2296409	0.63066
NM_001793.6(CDH3):c.813C>A (p.Thr271=)	rs2296408	0.62977
NM_001793.6(CDH3):c.1626T>C (p.Asn542=)	rs2296405	0.62283
NM_001793.6(CDH3):c.1956G>A (p.Lys652=)	rs2274239	0.61024
NM_001793.6(CDH3):c.2239C>A (p.Arg747=)	rs17715450	0.53279
NM_001793.6(CDH3):c.160+117G>A	rs2236393	0.44521
NM_001793.6(CDH3):c.247-38A>G	rs1952048	0.43462
NM_001793.6(CDH3):c.2281-45A>C	rs3114409

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