List of variants in gene EVC2 reported as benign by Eurofins NTD LLC (GA)

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_147127.5(EVC2):c.3507C>T (p.His1169=)	rs12511039	0.28547
NM_147127.5(EVC2):c.3557+10G>A	rs116218656	0.02138
NM_147127.5(EVC2):c.2047-9A>T	rs73198154	0.00366
NM_147127.5(EVC2):c.2601C>T (p.Ala867=)	rs116514447	0.00357
NM_147127.5(EVC2):c.2029C>A (p.Arg677=)	rs73198165	0.00341
NM_147127.5(EVC2):c.3659+8T>C	rs200119306	0.00270
NM_147127.5(EVC2):c.1711-11_1711-10del	rs35103377
NM_147127.5(EVC2):c.3272+8G>A	rs201800139

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