List of variants in gene NEB reported as benign by Genetic Services Laboratory, University of Chicago

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_001164508.2(NEB):c.3147+5G>A	rs74859201	0.01118
NM_001164508.2(NEB):c.21044C>G (p.Ser7015Cys)	rs62167164	0.00935
NM_001164508.2(NEB):c.20078C>T (p.Thr6693Ile)	rs35707762	0.00734
NM_001164508.2(NEB):c.3191A>G (p.Tyr1064Cys)	rs187343008	0.00681
NM_001164508.2(NEB):c.9865G>A (p.Gly3289Ser)	rs75639119	0.00460
NM_001164508.2(NEB):c.12C>T (p.Asp4=)	rs117178114	0.00119
NM_001164508.2(NEB):c.20089G>A (p.Gly6697Arg)	rs201071685	0.00001
NM_001164508.2(NEB):c.14734A>G (p.Asn4912Asp)	rs10909569

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