List of variants in gene NEXMIF reported as likely 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_001008537.3(NEXMIF):c.2598C>A (p.Ser866=)	rs41298498	0.01502
NM_001008537.3(NEXMIF):c.151C>A (p.Pro51Thr)	rs145018752	0.00705
NM_001008537.3(NEXMIF):c.4509T>C (p.Pro1503=)	rs41303725	0.00055
NM_001008537.3(NEXMIF):c.2098G>C (p.Val700Leu)	rs141776597	0.00038
NM_001008537.3(NEXMIF):c.1854G>A (p.Glu618=)	rs142687313	0.00012
NM_001008537.3(NEXMIF):c.4338G>A (p.Lys1446=)	rs200805356	0.00007
NM_001008537.3(NEXMIF):c.2669C>T (p.Pro890Leu)	rs377201508	0.00005
NM_001008537.3(NEXMIF):c.3637G>A (p.Gly1213Ser)	rs757442837	0.00003

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